Submitted Successfully!
To reward your contribution, here is a gift for you: A free trial for our video production service.
Thank you for your contribution! You can also upload a video entry or images related to this topic.
Version Summary Created by Modification Content Size Created at Operation
1
Sofia Lima
 -- 3909 2022-04-21 17:35:31 |
2 format correct
Vivi Li
 Meta information modification 3909 2022-04-22 05:08:04 |

Video Upload Options

We provide professional Video Production Services to translate complex research into visually appealing presentations. Would you like to try it?
No, upload directly Yes

Confirm

Are you sure to Delete?
Yes No
Cite
If you have any further questions, please contact Encyclopedia Editorial Office.
Lima, S.; , .; Gameiro, P.; Reis, S. Cutaneous Flavonoid Delivery System. Encyclopedia. Available online: https://encyclopedia.pub/entry/22130 (accessed on 16 November 2024).
Lima S,  , Gameiro P, Reis S. Cutaneous Flavonoid Delivery System. Encyclopedia. Available at: https://encyclopedia.pub/entry/22130. Accessed November 16, 2024.
Lima, Sofia, , Paula Gameiro, Salette Reis. "Cutaneous Flavonoid Delivery System" Encyclopedia, https://encyclopedia.pub/entry/22130 (accessed November 16, 2024).
Lima, S., , ., Gameiro, P., & Reis, S. (2022, April 21). Cutaneous Flavonoid Delivery System. In Encyclopedia. https://encyclopedia.pub/entry/22130
Lima, Sofia, et al. "Cutaneous Flavonoid Delivery System." Encyclopedia. Web. 21 April, 2022.
Cutaneous Flavonoid Delivery System
Edit
This entry is adapted from the peer-reviewed paper 10.3390/antiox10091376

Flavonoids are one of the vital classes of natural polyphenolic compounds abundantly found in plants. Due to their wide range of therapeutic properties, which include antioxidant, anti-inflammatory, photoprotective, and depigmentation effects, flavonoids have been demonstrated to be promising agents in the treatment of several skin disorders. However, their lipophilic nature and poor water solubility invariably lead to limited oral bioavailability. In addition, they are rapidly degraded and metabolized in the human body, hindering their potential contribution to the prevention and treatment of many disorders. Thus, to overcome these challenges, several cutaneous delivery systems have been extensively studied. Topical drug delivery besides offering an alternative administration route also ensures a sustained release of the active compound at the desired site of action. Incorporation into lipid or polymer-based nanoparticles appears to be a highly effective approach for cutaneous delivery of flavonoids with good encapsulation potential and reduced toxicity.

antioxidant inflammation skin research topical delivery transdermal delivery

1. Introduction

For centuries, flavonoids have been used to treat various human diseases, and despite the fast-growing development of new and innovative synthetic drugs, continuous use of these natural compounds has prevailed to this day [1][2]. Flavonoids are one of the key classes of bioactive compounds abundantly found in plants and have a general structure of a 15-carbon backbone, consisting of two benzene rings connected by a 3-carbon bridge, which forms a heterocycle. They are low-molecular-weight polyphenolic compounds derived from plant metabolites, and the presence of different substitutes creates different subclasses (Figure 1) [3][4][5]. Due to their broad spectrum of biological activity and attractive pharmacological properties, which include antioxidant, anti-inflammatory, antiproliferative, photoprotective, and antiaging effects, flavonoids have been explored as a therapeutic option towards a great number of diseases, including several skin disorders [6][7]. However, their lipophilic nature, which results in a reduced capacity to be orally absorbed, and the fact that they undergo extensive first-pass metabolism and rapid elimination hamper their oral bioavailability [8][9][10]. Thus, alternative research focuses on the development of the cutaneous delivery of flavonoids, with high patient compliance and potential to surpass drawbacks associated with oral and parental routes of administration. Although skin acts as a physical barrier to drug absorption, the development of delivery systems, such as nanoparticles, hydrogels, and microneedles, allows for the delivery of both hydrophilic and lipophilic compounds as well as drugs with shorter half-time and limited therapeutic index. This results in a higher bioavailability at the target site under a controlled release rate and avoids interactions with gastric and intestinal fluids as well as flavonoid degradation [11][12].
Figure 1. Classification of flavonoids based on their chemical structure.

2. Bioavailability of Flavonoids

One of the major concerns regarding the use of flavonoids as therapeutic agents is their relatively low bioavailability. Even in the presence of a large daily intake of flavonoids in dietary sources, their plasma and tissue concentrations are often insufficient to exert the desired pharmacological effects [3]. Due to several factors that include chemical structure and molecular weight, relatively low water solubility, absorption and metabolism in the gastrointestinal tract, lack of site specificity in distribution, and rapid elimination, flavonoids have generally low bioavailability, which largely affects their therapeutic potential. Moreover, this class of compounds is highly susceptive to degradation upon oxygen exposure, temperature changes, ultraviolet radiation, or pH change [13][14][15].
After being absorbed by the intestinal epithelium, flavonoids undergo extensive biotransformation into conjugated products, namely glucuronides, sulphates, and methylated derivatives, first in the intestine and then in the liver, where they are secreted into bile [16][17]. Thus, the bioavailability and the subsequent cell and tissue accumulation of the different flavonoids essentially depend on the multidrug-resistance-associated proteins (MRP-1 and MRP-2), ubiquitously expressed as ATP-dependent efflux transporters. The actual flux of a flavonoid from the gut lumen to the blood stream and the various organs depends on the tissue distribution of MRP-1 and MRP-2 as well as on their substrate’s affinity. This metabolic pathway is called phase III metabolism. However, it appears that certain phase II metabolic derivates of flavonoids can act as competitive substrates of the MRP-mediated membrane transporters and the potential use of flavonoids as a mean to overcome transporter-mediated chemotherapy resistance due to the frequent overexpression of MRP in several types of cancer is based on this property. The intestinal absorption of quercetin, for instance, is favored in the aglycone form, and its metabolism in the gut and liver appears to be relatively high, so that less than 2% of ingested quercetin is recovered on the plasma [3]. Additionally, after oral administration of flavonoids, a significant amount can reach the colon and can interact with microbiota. Microbiota can, for instance, metabolize some flavonoids to smaller phenolic compounds with similar biological effects and improved bioavailability; however, on the other hand, it can also extensively metabolize flavonoids via the glucuronidase and sulfatase enzymes, cleaving the heterocycle break and producing inert polar compounds that are rapidly excreted without producing any biological effect [13].
In addition, flavonoids have been reported to significantly inhibit the activity of the cytochrome P450 system, which can result in an increase of the half-life and concentration of many drugs, thus enhancing their toxicity and side effects [18]. Flavonoids such as quercetin, ECG, EGCG, and sylibin have been shown to downregulate the cytochrome CYP3A4, which is the major cytochrome P450 isoenzyme in the intestine and is responsible for the metabolism of approximately 50% of all prescribed drugs, thus increasing the risk of potential toxicity, especially of drugs with a limited therapeutic window [19]. Flavonoids can also interact with ATP-binding cassette (ABC) transporters, inhibiting them, which can increase the bioavailability of poorly available drugs, on the one hand, but it can also potentiate the toxicity of other ABC transporters substrates [20]. Thus, flavonoid encapsulation in effective nano-carrier systems can not only improve their pharmacokinetics and therapeutic potential but also avoid enhancement of the toxicity and side effects of drugs that can concomitantly be administrated with these compounds [13].
The rapid metabolic elimination of flavonoids, together with the evidence that they are able to interact with the metabolism of other drugs, highlights the need to develop novel ways to improve the delivery of flavonoids. Cutaneous administration emerges as an alternative option to common oral and parenteral routes [21][22]. Skin drug delivery is one of the most preferred administration routes with higher patient compliance and satisfaction. The advantages also include the avoidance of liver first pass metabolism effects, metabolic degradation associated with oral administration, and minimal systemic side effects.

3. The Need for Nanocarriers in Cutaneous Flavonoid Delivery

Despite flavonoids’ pharmacological potential, dietary flavonoids present several disadvantages, hindering their clinical potential. In addition, the fact that flavonoids can suffer an enhanced complexation or precipitation when ingested with other food components as well as degradation by microbiota greatly reduces their bioavailability and stability. On that matter, cutaneous delivery is one of the most advantageous routes in overcoming the challenges associated with flavonoid administration [3][13].
Nonetheless, the impermeable nature of the skin presents a serious challenge to cutaneous delivery, where in most of the cases the therapeutic effect produced by the conventional drug dosage is not sufficiently effective. Thus, the development of nano-engineered delivery systems for flavonoids capable of increasing the solubility and bioavailability and of providing a site-specific delivery with improved pharmacokinetic properties is imperative. Thus far, gels are the most common form of topical drug administration, including hydrogels and olegels. However, other delivery systems such as lipid and polymeric nanoparticles, microparticles, and transferosomes, among others, are currently being developed (Figure 2). These carriers can later be formulated into creams and gels, improving patient compliance [5].
Figure 2. Schematic representation of nano-delivery systems used for topical skin delivery.

4. Cutaneous Delivery Systems of Flavonoids for Treatment of Skin Pathologies

Cutaneous delivery of flavonoids is a powerful strategy to avoid systemic toxicity while restricting the therapeutic effects to the specific site of action. However, one of the major challenges that a topical delivery system faces is the ability to overcome the SC barrier against foreign substances [5]. In addition, most flavonoids are highly lipophilic compounds and their permeation across the SC into viable skin layers is hindered by their affinity for SC components and the tendency to be retained in this layer. Thus, there has been a growing interest in the use of nanotechnology as a strategy for a more efficient flavonoid delivery to the human body (Figure 3). Nano-delivery systems are in fact excellent tools to overcome the challenges associated not only with the cutaneous absorption of the drug per se but also with flavonoid pharmacology, including low solubility, short half-life, and poor bioavailability [5][23].
Figure 3. Limitations and advances on cutaneous flavonoid delivery.

4.1. Examples of Nanocarriers Designed for Flavonol Cutaneous Delivery

Flavonols are O-glycosidic ketonic compounds with a sugar moiety at the 3-position that act as powerful antioxidants, protecting the skin from ROS formation. Compounds belonging to this family of flavonoids are quercetin, kaempferol, and myricetin, among others [24].
Quercetin, one of the best studied and most common flavonoid found in nature, was shown to have poor permeability across excised human skin [4]. For that, this flavonoid has been incorporated into different delivery systems, including nanoemulsions, nanocapsules, lipid nanoparticles, and microemulsions, to increase its solubility and skin permeability [5]. Casagrande and colleagues incorporated quercetin into two different oil-in-water emulsions with a distinct lipid content in order to evaluate their potential application as a topical delivery system. The in vivo results demonstrated that these formulations were an effective vehicle for topical application of quercetin with the goal of controlling ultraviolet B (UVB)-induced skin damage [4][25]. Based on these results, other studies were conducted to design novel delivery systems to increase quercetin effectiveness when topically applied. For example, quercetin was incorporated into a liquid, crystalline formulation and the influence of this vehicle in the antioxidant activity of this flavonoid was evaluated in vitro. The presence of a liquid, crystalline structure allowed for an easier diffusion through the skin and a considerable solubilizing capacity for both oil- and water-soluble compounds. Scalia and colleagues also demonstrated that the incorporation of quercetin in lipid microparticles improved its photostability and chemical stability as well as its biocompatibility [26][27]. In another study, Tan and colleagues investigated the potential of using lecithin-chitosan nanoparticles as a topical delivery system for quercetin. Compared with quercetin in its free form, the quercetin-loaded nanoparticles displayed higher permeation ability and significant accumulation of quercetin in the skin, particularly in the epidermis. In addition, microstructure observations of the skin surface following administration showed that the interaction between constituents of the nanoparticles and the skin surface markedly changed the morphology of the SC and disrupted the corneocyte layers, therefore facilitating permeation and accumulation of quercetin in the skin [28].
Nan and colleagues evaluated the efficacy of topically applying quercetin-loaded chitosan nanoparticles against UVB radiation. The authors demonstrated that quercetin, if entrapped into chitosan nanoparticles, could be efficiently up taken by HaCaT cells (keratinocytes) and could easily permeate through the epidermis layer while displaying better stability and lower cytotoxicity. Moreover, they also found that quercetin-loaded nanoparticles could enhance the effects of this flavonoid when inhibiting the NF-kB/COX-2 signaling pathway as well as when ameliorating the skin edema caused by UVB radiation [29].
Bose and Michniak-Kohn developed a solvent-free NLC formulation of quercetin using probe ultrasonication and evaluated the feasibility for topical delivery. Formulation factors such as the nature of the lipid (solid/combination of solid and liquid) in the SLN and NLC systems and the drug loading capacity were evaluated to produce the optimal formulation with an adequate physical stability. Overall, the NLC system showed the highest improvement in the topical delivery of quercetin, manifested by the amount of quercetin retained in full-thickness human skin compared with a control formulation with a similar composition and particle size in the micrometer range, thus demonstrating the feasibility of NLC systems for improved cutaneous delivery of this compound [30].
Penetration enhancer containing vesicles (PEVs) are also known to be powerful enhancers for dermal delivery due to the presence of both phospholipids and penetration enhancers (PE), which provide a synergistic effect on skin permeation. PE increases the fluidity of the lipids of the SC, facilitating the delivery of drug-loaded vesicles and its subsequent diffusion through the skin [5]. Hence, in 2011, Chessa and colleagues developed quercetin-loaded PEVs, formulated using four different hydrophilic PE, and characterized them by size, surface charge, loading capacity, and morphological and viscoelastic features. In addition, their penetration capability and distribution through pig skin were assessed to obtain the optimal formulation for the delivery of quercetin to the skin [31]. In another study, performed by Caddeo and colleagues, quercetin-loaded phospholipid vesicles, in particular liposomes and PEVs, were developed in order to study their efficacy on 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced skin inflammation. In vivo results demonstrated that the vesicles, in particular PEVs, were capable of delivering the drug to the inflammation site, that is the dermis, inhibiting oxidative stress and leukocyte accumulation as well as stimulating the repair of skin damaged induced by TPA. Through this work, the authors highlighted the use of vesicular systems, particularly PEVs, as a delivery vehicle for flavonoids, with a therapeutic potential to treat inflammatory skin disorders [32].
Kaempferol is another well-known flavonol with antioxidant, anti-inflammatory, anticancer, and antiallergic properties [33]. In fact, Wang and colleagues reported that kaempferol inhibited the iNOS mRNA expression and prostaglandin E2 production in a dose-dependent manner, by inhibiting in part the NF-kB signaling pathway [34]. Furthermore, Park et al. reported that kaempferol was also able to inhibit the activation of inflammatory NF-kB transcription factor via nuclear factor-inducing kinase (NIK)/IkB kinase (IKK) and MAPKs in aged rat kidney [35]. Nonetheless, studies have shown that this flavonoid undergoes excessive first pass metabolism and, as a consequence, displays a bioavailability rate of only 2%, thus making it a good candidate for cutaneous application [33]. Keeping that in mind, Yun Chao and colleagues developed submicron emulsions to be employed as a delivery system for the topical application of kaempferol. These submicron emulsion systems are oil-in-water dispersions with small droplet sizes in the range of 100–600 nm. In comparison with traditional drug delivery vehicles, they are easy to manufacture, are more thermodynamically stable, and exhibit enhanced drug solubilization as well as increased drug permeation rates. Additionally, submicron emulsions were demonstrated to be a potential vehicle for the transdermal and topical delivery of lipophilic and hydrophilic drugs. In the study, kaempferol-loaded submicron emulsions with different water/oil/surfactant/cosurfactant ratios were prepared, and different physiochemical properties (e.g., viscosity, droplet size, permeation rate, lag time, and deposition amount in skin) were determined in order to evaluate the effectiveness of this delivery system for the cutaneous application of kaempferol. Overall, the authors demonstrated that, based on the permeation parameters, including the increase in the cumulative amount of drug over 12 h and deposition in the skin, in addition to a shorter lag time, submicron emulsions may be a promising vehicle for cutaneous application of kaempferol [33].

4.2. Examples of Nanocarriers Designed for Other Flavonoid Classes’ Topical Delivery

Isoflavones, are naturally occurring isoflavonoids mainly found in soybeans, soy foods, and legumes. They are non-steroidal compounds that act as phytoestrogens as they exert pseudohormonol activity by binding to estrogen receptors in mammals. The most common isoflavones are genistein and daidzein [5]. Huang and colleagues assessed the potential topical delivery and dermal use of soy isoflavones genistein and daidzein, using α-terpineol and oleic acid as PE, both in vitro and in vivo. As demonstrated in vivo, there was an increase in the uptake of genistein an daidzein, with no toxic effects, and a decrease in the erythema. In vitro studies showed an inhibition of UVB-induced intracellular H2O2 production and the consequent protection of keratinocytes against UVB radiation, suggesting that a reduction in photodamage to the skin via the topical application of antioxidants could be an efficient way to enrich the endogenous cutaneous protection system [34][36].
Apigenin is a hydrophobic, polyphenolic flavonoid known to possess antioxidant, antimicrobial, anti-inflammatory, antiviral, antidiabetic, and tumor inhibitory activities. In particular, this flavonoid was demonstrated to act as a chemo-preventive by inhibiting the enzyme CYP2C and by preventing the metabolism of many drugs and xenobiotics. Similar to the already mentioned flavonoids, the clinical potential of apigenin is suppressed by its poor aqueous solubility, low oral bioavailability, and rapid metabolism. Thus, the development of novel formulations is a necessary step to overcome these limitations and to improve apigenin delivery [5]. On that matter, several formulations have been developed so far, including liposomes, nanocrystal gel formulations, and self-micro-emulsifying drug delivery systems. Munyendo and colleagues reported that the formulation of D-α-tocopherol acid and polyethylene glycol 1000 succinate (TPGS) stabilized the mixed micelles of apigenin and phospholipids, creating an effective drug delivery vehicle capable of enhancing the bioavailability of this flavonoid [37]. Karthivashan and colleagues prepared “flavonosomes”, which are phytosomes loaded with multiple flavonoids, using phosphatidylcholine as a carrier and evaluated their in vitro pharmacokinetics and toxicity [38]. Shen and co-workers evaluated a novel topical delivery system for apigenin by using soy lecithin-based ethosomes, demonstrating a higher skin targeting capacity and a significant reduction in COX-2 levels in mouse skin inflammation induced by UVB light [39].
Luteolin is another promising flavonoid with potential antiarthritic activity. In addition, due to its lipophilicity, it can be used in topical formulations to treat psoriasis [40]. Niosomes are non-ionic surfactant-based colloidal systems that have the ability to encapsulate both hydrophobic and hydrophilic drugs. Abidin and co-workers prepared luteolin-loaded niosomes using different non-ionic surfactants and characterized them for their in vitro and in vivo antiarthritic activity. The optimized formulation was later converted into gel using Carbopol as a gelling agent for enhanced transdermal luteolin delivery. The in vivo bioactive studies revealed that the niotransgel formulation of luteolin was able to provide good antiarthritic activity, with the results being comparable with standard diclofenac gel formulation [41]. In another study, Shin and colleagues, established a nanoemulsion-based follicular delivery system, in which luteolin was incorporated into oil-in-water nanoemulsions. In vivo studies proved that these luteolin-loaded nanoemulsions possessed hair-growth promotion ability. In fact, when nanoemulsions are formed by the assembly of amphiphilic polymers at the oil/water (O/W) interface, they provide an efficient system for the encapsulation of poorly water-soluble substances, resulting in better bioavailability, accurate dosing, and minimal side effects [42].
Catechins are a group of flavonoids that belong to the flavanol family and are present in high concentrations in a variety of plant-based fruits, vegetables, and beverages. Belonging to this family are catechin, epicatechin (EG), and EGCG. EGCG, in particular, has captured a lot of attention due to its broad spectrum of biological properties, including antioxidant, photoprotective, antiviral, and antibacterial as well as anticancer and neuroprotective effects. Nevertheless, its clinical use has been limited due to its poor systemic absorption and low bioavailability [5]. With the goal to overcome this problem and to increase EGCG clinical applicability, Avadhani and co-workers developed nano-transfersomal formulations of EGCG for an efficient permeation into the SC and delivery into the skin [43]. In addition, hyaluronic acid (HA) was also encapsulated in the transfersomes not only because it is widely distributed in connective tissues and is a main component of the extracellular matrix but also because it is a non-irritating biopolymer and antiaging agent with high biocompatibility, specific viscoelasticity, and hydration and lubrification properties. The optimized transfersomal formulation containing EGCG and HA displayed a high free radical scavenging effect while showing no cell toxicity. In addition, the formulation was able to suppress the MDA and ROS levels to a significant extent in human keratinocytes as well as the expression levels of MMP-2 and MMP-9. The encapsulation of EGCG in the transfersomes resulted in higher skin permeation and deposition of this flavonoid in the skin, compared with plain EGCG. Interestingly, the co-entrapment of HA in the formulation increased both the skin permeation and deposition of EGCG, thus demonstrating that this system constitutes a useful and effective EGCG cutaneous delivery vehicle, with synergistic antiaging and antioxidant benefits [43].
Fang and colleagues assessed the possibility of using multilamellar phosphatidylcholine (PC) liposomes studied for topical and intratumor delivery administration of catechin, EC, and EGCG in nude mice [44][45]. The authors showed that the inclusion of anionic species such as deoxycholic acid and dicetyl phosphate increased the encapsulation of the catechins and the permeability of the lipid bilayers. EGCG performed differently due to its higher lipophilicity. In addition, the authors reported an even higher EGCG encapsulation for deoxycholic acid-liposomes prepared in the presence of 15% ethanol as well as an increased catechin in vitro and in vivo skin permeation and deposition in basal cell carcinomas compared with both the free form and ethanol-free liposomes. This might be attributed to the fact that ethanol-enriched liposomes penetrate easily in the skin due to the increased elasticity conferred by the insertion of alcohol into the PC membranes. The results showed that optimization of the physicochemical features and composition of liposomes could control and improve the delivery of catechins. Moreover, the results suggested that the intratumor administration of liposomes might be an effective approach for the local treatment of solid tumors [44][45].
Overall, there are several strategies that can be adopted to increase the solubility and subsequent bioavailability of flavonoids with therapeutic potential. Although much progress has been recently made, novel drug delivery systems suitable for an optimized topical application should continue to be explored [21][46][47][48][49]. A summary of the therapeutic application of flavonoids and the different nanocarriers used to enhance their delivery to the skin is described in Table 1.
Table 1. In vitro and in vivo studies using different nanocarriers for enhanced topical delivery of flavonoids to the skin.
Flavonoid Nanoformulation Skin Model Therapeutic Application Ref.
Quercetin Solid lipid
nanoparticles		 Human skin Delay UVB radiation-mediated cell damage and necrosis [30]
Non-ionic emulsion with high lipid content Pig ear skin Inhibition of UVB-induced cutaneous oxidative stress and inflammation [4]
Anionic emulsion with low lipid content Pig ear skin Inhibition of UVB-induced cutaneous oxidative stress and inflammation [4]
Lecithin-chitosan nanoparticles Male Kunming mice Topical delivery system with a wide range of applications [28]
Lipid microparticles n.a. Enhance quercetin stability in topical formulations [27]
Colloidal silica
emulsion		 Human skin Optimization of a formulation with enhance penetration into human SC [48]
Chitosan nanoparticles HaCaT cells Potential therapeutic agent for topical use against UVB radiation [29]
Penetration Enhancer containing Vesicles (PEVs) New born pig skin New formulation for dermal delivery of quercetin, with various therapeutic applications [31]
Polylactide nanocapsules; Multilamellar liposomes; Niosomes Subcutaneous injection in amistogote-infected hamsters Antileishmanial agent [3][49]
Liposomes with penetration enhancing vesicles (PEV) Female CD-1 mice Anti-inflammatory agent [5][49]
Lipid nanocapsules Acute monocytic leukemia cell line (THP1–1 cell) Antioxidant, anti-inflammatory agent [5][50]
Nanoparticle suspension Mice Antioxidant agent [5][41]
Catechins Multilamellar phosphatidylcholine-liposomes Female nude mouse (Balb/c-nu, 6–8 weeks old) Use of liposomes for the local delivery, including skin and tumor deposition, of polyphenols [3][43]
Ethanol enriched liposomes Female nude mouse (Balb/c-nu, 6–8 week) Antioxidant and chemopreventive activity [44]
Cream Iranian rabbits Wound healing effect [5][51]
Tansfersomes containing EGCG and hyaluronic acid (HA) HaCaT cells Synergize the UV radiation-protective ability of EGCG and HA along with imparting antioxidant and antiaging effects [5][42]
Genistein Nanoemulsion Pig ear skin New formulation for dermal delivery of genistein, with various therapeutic applications [3][52]
Kaempferol Submicron emulsions Sprague Dawley rat Promising vehicle for topical kaempferol application [33]
Resveratrol Solid lipid
Nanoparticles		 Porcine skin Protection from photodegradation [53]
Resveratrol + curcumin Lipid-core
Nanocapsules		 Human skin Increase skin delivery of resveratrol [54]
Niosomes Cell rabbit skin Increase skin delivery of resveratrol
Increased antioxidant activity		 [55]
Hesperetin, hesperidin Microemulsion Guinea pigs Whitening effect [5][56]
Topical matrix film Albino rabbits Release of hesperetin in posterior of eye [5][57]
Microemulsion based ointment Wistar rats Skin irritation [5][58]
Naringenin Gel HRS/J mice Antioxidant and anti-inflammatory agent [5][54]
Nanoparticles Wistar rats Photoprotective, antioxidant agent [5][54]
Apigenin Phospholipid phytosomes Albino rats Antioxidant agent [5][59]
Ethosomes Konmin mice Anti-inflammatory agent [5][60]
Anthocyanin Niosome gel Male Wistar rats Anti-inflammatory agent [5][61]
Luteolin Luteolin in olive oil ICR mice Anti-inflammatory agent [5][62]
Luteolin-loaded niosomes/Niosomal transgel Albino Wistar rats Treatment of arthritis [40]
Nanoemulsion C57BL/6 mice Growth promoting effect [41]

References

  1. Kumar, S.; Pandey, A.K. Chemistry and Biological Activities of Flavonoids: An Overview. Sci. World J. 2013, 4, 1–16.
  2. Panche, A.N.; Diwan, A.D.; Chandra, S.R. Flavonoids: An overview. J. Nutr. Sci. 2016, 5, e47.
  3. Leonarduzzi, G.; Testa, G.; Sottero, B.; Gamba, P.; Poli, G. Design and Development of Nanovehicle-Based Delivery Systems for Preventive or Therapeutic Supplementation with Flavonoids. Curr. Med. Chem. 2009, 17, 74–95.
  4. Verri, W.A.; Vicentini, F.T.M.C.; Baracat, M.M.; Georgetti, S.R.; Cardoso, R.D.R.; Cunha, T.M.; Ferreira, S.H.; Cunha, F.Q.; Fonseca, M.J.V.; Casagrande, R. Studies in Natural Products Chemistry, 1st ed.; Elsevier: Amsterdam, The Netherlands, 2012; Volume 36.
  5. Nagula, R.L.; Wairkar, S.J. Recent advances in topical delivery of flavonoids: A review. Control. Release 2019, 296, 190–201.
  6. Domaszewska-Szostek, A.; Puzianowska-Kuźnicka, M.; Kuryłowicz, A. Flavonoids in Skin Senescence Prevention and Treatment. Int. J. Mol. Sci. 2021, 22, 6814.
  7. Yang, B.; Liu, H.; Yang, J.; Gupta, V.K.; Jiang, Y. New insights on bioactivities and biosynthesis of flavonoid glycosides. Trends Food Sci. Technol. 2018, 79, 116–124.
  8. Yang Wang, T.; Li, Q.; Shun Bi, K. Bioactive flavonoids in medicinal plants: Structure, activity and biological fate. Asian J. Pharm. Sci. 2017, 13, 12–23.
  9. Rengasamy, K.R.R.; Khan, H.S.; Gowrishankar, S.; Lagoa, R.J.L.; Mahomoodally, F.M.; Khan, Z.; Suroowan, S.; Tewari, D.; Zengin, G.; Hassan, S.T.S.; et al. The role of flavonoids in autoimmune diseases: Therapeutic updates. Pharmacol. Ther. 2018, 194, 107–131.
  10. Perez-Vizcaino, F.; Fraga, C.G. Research trends in flavonoids and health. Arch. Biochem. Biophys. 2018, 646, 107–112.
  11. Shelke, S.J.; Shinkar, D.M.; Saudagar, R.B. Topical gel: A novel approach for development of topical drug delivery system. Int. J. Pharm. Technol. 2013, 5, 2739–2763.
  12. Menaa, F.; Menaa, A.; Menaa, B. Polyphenols Nano-Formulations for Topical Delivery and Skin Tissue Engineering. In Polyphenols in Human Health and Disease; Elsevier Inc: Amsterdam, The Netherlands, 2014; pp. 839–848.
  13. Khan, H.; Ullah, H.; Martorell, M.; Valdes, S.E.; Belwal, T.; Tejada, S.; Sureda, A.; Kamal, M.A. Flavonoids nanoparticles in cancer: Treatment, prevention and clinical prospects. Semin. Cancer Biol. 2021, 69, 200–211.
  14. Ruenroengklin, N.; Zhong, J.; Duan, X.; Yang, B.; Li, J.; Jiang, Y. Effects of Various Temperatures and pH Values on the Extraction Yield of Phenolics from Litchi Fruit Pericarp Tissue and the Antioxidant Activity of the Extracted Anthocyanins. Int. J. Mol. 2008, 9, 1333–1341.
  15. Palafox-Carlos, H.; Ayala-Zavala, J.F.; González-Aguilar, G.A. The role of dietary fiber in the bioaccessibility and bioavailability of fruit and vegetable antioxidants. J. Food Sci. 2011, 76, R6–R15.
  16. Li, C.; Lee, M.J.; Sheng, S.; Meng, X.; Prabhu, S.; Winnik, B.; Huang, B.; Chung, J.Y.; Yan, S.; Ho, C.T.; et al. Structural identification of two metabolites of catechins and their kinetics in human urine and blood after tea ingestion. Chem. Res. Toxicol. 2000, 13, 177–184.
  17. Lambert, J.D.; Sang, S.; Yang, C.S. Biotransformation of green tea polyphenols and the biological activities of those metabolites. Mol. Pharm. 2007, 4, 819–825.
  18. Schubert, W.; Eriksson, U.; Edgar, B.; Cullberg, G.; Hedner, T. Flavonoids in grapefruit juice inhibit the in vitro hepatic metabolism of 17β-estradiol. Eur. J. Drug Metab. Pharmacok. 1995, 20, 219–224.
  19. Ramadon, D.; McCrudden, M.T.C.; Courtenay, A.J.; Donnelly, R.F. Enhancement strategies for transdermal drug delivery systems: Current trends and applications. Drug Deliv. Transl. Res. 2021, 11, 1–34.
  20. Cermak, R.; Wolffram, S. Effect of dietary flavonoids on pathways involved in drug metabolism. Expert Opin. Drug Metab. Toxicol. 2008, 4, 17–35.
  21. Rahman, H.S.; Othman, H.H.; Hammadi, N.I.; Yeap, S.K.; Amin, K.M.; Samad, N.A.; Alitheen, N.B. Novel drug delivery systems for loading of natural plant extracts and their biomedical applications. Int. J. Nanomed. 2020, 15, 2439.
  22. Jain, K.K. Nanomedicine: Application of nanobiotechnology in medical practice. Med. Princ. Pract. 2008, 17, 89–101.
  23. Kreuter, J. Nanoparticles. In Encyclopaedia of Pharmaceutical Technology; Marcel Dekker Inc: New York, NY, USA, 1994.
  24. Casagrande, R.; Georgetti, S.R.; Verri, W.A., Jr.; Borin, M.F.; Lopez, R.F.; Fonseca, M.J. In vitro evaluation of quercetin cutaneous absorption from topical formulations and its functional stability by antioxidant activity. Int. J. Pharm. 2007, 328, 183–190.
  25. Casagrande, R.; Georgetti, S.R.; Verri, W.A., Jr.; Dorta, D.J.; dos Santos, A.C.; Fonseca, M.J. Protective effect of topical formulations containing quercetin against UVB-induced oxidative stress in hairless mice. J. Photochem. Photobiol. 2006, 84, 21–27.
  26. Vicentini, F.T.; Casagrande, R.; Verri, W.A., Jr.; Georgetti, S.R.; Bentley, M.V.; Fonseca, M.J. Quercetin in lyotropic liquid crystalline formulations: Physical, chemical and functional stability. AAPS Pharm. Sci. Technol. 2008, 9, 591–596.
  27. Scalia, S.; Mezzena, M.J. Incorporation of quercetin in lipid microparticles: Effect on photo-and chemical-stability. Pharm. Biomed. Anal. 2009, 49, 90–94.
  28. Tan, Q.; Liu, W.; Guo, C.; Zhai, G. Design of self-assembling peptides and their biomedical applications. Int. J. Nanomed. 2011, 6, 1621.
  29. Nan, W.; Ding, L.; Chen, H.; Khan, F.U.; Yu, L.; Sui, X.; Shi, X. Discovery of the consistently well-performed analysis chain for SWATH-MS based pharmacoproteomic quantification. Front. Pharmacol. 2018, 9, 1–11.
  30. Bose, S.; Michniak-Kohn, B. Preparation and characterization of lipid based nanosystems for topical delivery of quercetin. Eur. J. Pharm. Sci. 2013, 48, 442–452.
  31. Chessa, M.; Caddeo, C.; Valenti, D.; Manconi, M.; Sinico, C.; Fadda, A.M. Effect of penetration enhancer containing vesicles on the percutaneous delivery of quercetin through new born pig skin. Pharmaceutics 2011, 3, 497–509.
  32. Caddeo, C.; Díez-Sales, O.; Pons, R.; Fernàndez-Busquets, X.; Fadda, A.M.; Manconi, M. Topical Anti-Inflammatory Potential of Quercetin in Lipid-Based Nanosystems: In Vivo and In Vitro Evaluation. Pharmaceut. Res. 2014, 31, 959–968.
  33. Chao, Y.; Huang, C.-T.; Fu, L.-T.; Huang, Y.-B.; Tsai, Y.-H.; Wu, P.-C. The Effect of Submicron Emulsion Systems on Transdermal Delivery of Kaempferol. Chem. Pharmaceut. Bull. 2012, 60, 1171–1175.
  34. Wang, L.; Tu, Y.C.; Lian, T.W.; Hung, J.T.; Yen, J.H.; Wu, M.J. Distinctive Antioxidant and Antiinflammatory Effects of Flavonols. J. Agric. Food Chem. 2006, 54, 9798–9804.
  35. Simões, S.; Moreira, J.N.; Fonseca, C.; Düzgüneş, N.; de Lima, M.C. On the formulation of pH-sensitive liposomes with long circulation times. Adv. Drug Deliv. Rev. 2004, 56, 947–965.
  36. Huang, Z.-R.; Hung, C.-F.; Lin, Y.-K.; Fang, J.-Y. In vitro and in vivo evaluation of topical delivery and potential dermal use of soy isoflavones genistein and daidzein. Int. J. Pharm. 2008, 364, 36–44.
  37. Munyendo, W.L.L.; Zhang, Z.; Abbad, S.; Waddad, A.Y.; Lv, H.; Baraza, L.D.; Zhou, J. Micelles of TPGS modified apigenin phospholipid complex for oral administration: Preparation, in vitro and in vivo evaluation. J. Biomed. Nanotechnol. 2013, 9, 2034–2047.
  38. Shen, L.N.; Zhang, Y.T.; Wang, Q.; Xu, L.; Feng, N.P. Enhanced in vitro and in vivo skin deposition of apigenin delivered using ethosomes. Int. J. Pharm. 2014, 460, 280–288.
  39. Karthivashan, G.; Masarudin, M.J.; Umar Kura, A.; Abas, F.; Fakurazi, S. Optimization, formulation, and characterization of multiflavonoids-loaded flavanosome by bulk or sequential technique. Int. J. Nanomed. 2016, 11, 3417–3434.
  40. Abidin, L.; Mujeeb, M.; Imam, S.S.; Aqil, M.; Khurana, D. Enhanced transdermal delivery of luteolin via non-ionic surfactant-based vesicle: Quality evaluation and anti-arthritic assessment. Drug Deliv. 2016, 23, 1069–1074.
  41. Shin, K.; Choi, H.; Song, S.K.; Yu, J.W.; Lee, J.Y.; Choi, E.J.; Lee, D.H.; Do, S.H.; Kim, J.W. Nanoemulsion Vehicles as Carriers for Follicular Delivery of Luteolin. ACS Biomat. Sci. Eng. 2018, 4, 1723–1729.
  42. Avadhani, K.S.; Manikkath, J.; Tiwari, M.; Chandrasekhar, M.; Godavarthi, A.; Vidya, S.M.; Hariharapura, R.C.; Kalthur, G.; Udupa, N.; Mutalik, S. Skin delivery of epigallocatechin-3-gallate (EGCG) and hyaluronic acid loaded nano-transfersomes for antioxidant and anti-aging effects in UV radiation induced skin damage. Drug Deliv. 2017, 4, 61–74.
  43. Fang, J.Y.; Hung, C.F.; Hwang, T.L.; Huang, Y.L. Physicochemical characteristics and in vivo deposition of liposome-encapsulated tea catechins by topical and intratumor administrations. J. Drug Target 2005, 13, 19–27.
  44. Fang, J.Y.; Hwang, T.L.; Huang, Y.L.; Fang, C.L. Enhancement of the transdermal delivery of catechins by liposomes incorporating anionic surfactants and ethanol. Int. J. Pharm. 2006, 310, 131–138.
  45. Bhia, M.; Motallebi, M.; Abadi, B.; Zarepour, A.; Pereira-Silva, M.; Saremnejad, F.; Santos, A.C.; Zarrabi, A.; Melero, A.; Jafari, S.M.; et al. Naringenin Nano-Delivery Systems and Their Therapeutic Applications. Pharmaceutics 2021, 13, 291.
  46. Nasr, M.; Al-Karaki, R. Nanotechnological Innovations Enhancing the Topical Therapeutic Efficacy of Quercetin: A Succinct Review. Curr. Drug Deliv. 2020, 17, 270–278.
  47. Guan, F.; Wang, Q.; Bao, Y.; Chao, Y. Anti-rheumatic effect of quercetin and recent developments in nano formulation. RSC Adv. 2021, 11, 7280–7293.
  48. Scalia, S.; Franceschinis, E.; Bertelli, D.; Iannuccelli, V. Comparative Evaluation of the Effect of Permeation Enhancers, Lipid Nanoparticles and Colloidal Silica on in vivo Human Skin Penetration of Quercetin. Skin Pharmacol. Physiol. 2013, 25, 57–67.
  49. Sarkar, S.; Mandal, S.; Sinha, J.; Mukhopadhyay, S.; Das, N.; Basu, M.K. Quercetin: Critical evaluation as an antileishmanial agent in vivo in hamsters using different vesicular delivery modes. J. Drug Target 2002, 10, 573–578.
  50. Hatahet, T.; Morille, M.; Shamseddin, A.; Aubert-Pouëssel, A.; Devoisselle, J.M.; Begu, S. Dermal quercetin lipid nanocapsules: Influence of the formulation on antioxidant activity and cellular protection against hydrogen peroxide. Int. J. Pharm. 2017, 518, 167–176.
  51. Tan, Q.; Liu, W.; Zhai, G. Preparation and evaluation of quercetin-loaded lecithin-chitosan nanoparticles for topical delivery. Int. J. Nanomed. 2011, 6, 1621–1630.
  52. Silva, A.P.; Nunes, B.R.; De Oliveira, M.C.; Koester, L.S.; Mayorga, P.; Bassani, V.L.; Teixeira, H.F. Development of topical nanoemulsions containing the isoflavone genistein. Pharmazie 2009, 64, 32–35.
  53. Carlotti, M.; Sapino, S.; Ugazio, E.; Gallarate, M.; Morel, S.J. Resveratrol in Solid Lipid Nanoparticles. Dispers. Sci. Technol. 2012, 33, 465–471.
  54. Friedrich, R.B.; Kann, B.; Coradini, K.; Offerhaus, H.L.; Beck, R.C.; Windbergs, M. Skin penetration behavior of lipid-core nanocapsules for simultaneous delivery of resveratrol and curcumin. Eur. J. Pharm. Sci. 2015, 78, 204–213.
  55. Tavano, L.; Muzzalupo, R.; Picci, N.; de Cindio, B. Co-encapsulation of lipophilic antioxidants into niosomal carriers: Percutaneous permeation studies for cosmeceutical applications. Colloids Surf. B. 2014, 114, 144–149.
  56. Tsai, Y.; Lee, K.; Huang, Y.; Huang, C. In vitro permeation and in vivo whitening effect of topical hesperetin microemulsion delivery system. Int. J. Pharm. 2010, 388, 257–262.
  57. Adelli, G.R.; Hingorani, T.; Punyamurthula, N.; Prachetan, S.; Majumdar, S. Evaluation of topical hesperetin matrix film for back-of-the-eye delivery. Eur. J. Pharm. Biopharm. 2015, 92, 74–82.
  58. Kilor, V.; Sapkal, N.; Vaidya, G. Design and development of novel microemulsion based topical formulation of Hesperidin. Int. J. Pharm. Pharm. Sci. 2015, 7, 142–148.
  59. Haritima, J. Papr reduction using scs-slm technique in stfbc mimo-ofdm. ARPN J. Eng. Appl. Sci. 2017, 12, 3218–3221.
  60. Telange, D.R.; Patin, A.T. Formulation and characterization of an apigenin-phospholipid phytosome (APLC) for improved solubility, in vivo bioavailability, and antioxidant potential. Eur. J. Pharm. Sci. 2016, 108, 36–49.
  61. Priprem, A.; Limsitthichaikoon, S.; Thappasarapong, S.; Complex, A.A. Preparation, Anti-inflammatory Activity of Topical Anthocyanins by Complexation and Niosomal Encapsulation. Int. J. Chem. Mol. Eng. 2015, 9, 133–137.
  62. Baolin, L.; Weiwei, W.; Ning, T. Topical Application of Luteolin Inhibits Scratching Behavior Associated with Allergic Cutaneous Reaction in Mice. Planta Med. 2005, 71, 424–428.
More
© Text is available under the terms and conditions of the Creative Commons Attribution (CC BY) license; additional terms may apply. By using this site, you agree to the Terms and Conditions and Privacy Policy.
Upload a video for this entry
Information
Subjects: Biochemical Research Methods
Contributors MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register :
Sofia Lima
,
,
Paula Gameiro
,
Salette Reis
View Times: 792
Entry Collection: Biopharmaceuticals Technology
Revisions: 2 times (View History)
Update Date: 22 Apr 2022
Table of Contents
    1000/1000
    Hot Most Recent
    ScholarVision Creations
    Feedback