| Version | Summary | Created by | Modification | Content Size | Created at | Operation |
|---|---|---|---|---|---|---|
| 1 | Helena Kang | -- | 170 | 2026-10-09 08:12:58 | | | |
| 2 | Helena Kang | Meta information modification | 170 | 2026-10-09 08:45:34 | | | | |
| 3 | Catherine Yang | -9 word(s) | 161 | 2026-10-09 08:46:20 | | |
A focused laser that ablates a micrometre-scale spot, coupled to a time-of-flight or related mass analyzer, defines laser microprobe mass spectrometry (LMMS, historically LAMMA). The microprobe geometry localizes the desorption and ionization event so that elemental and molecular ions from a selected microscopic volume are recorded [1]. Direct laser desorption from the neat solid may be compared with matrix-assisted desorption from the same microprobe, which changes the ion yield and fragmentation but not the spatial-probe definition [2]. Conceptual boundaries exclude bulk laser-desorption mass spectrometry without spatial selection, secondary-ion microprobes that use an ion beam, and optical laser microprobes that do not mass-analyze the ejecta. Essential features are a diffraction-limited or otherwise focused laser, a viewing system that registers the sampled spot, and a mass analyzer synchronized to the laser pulse [3]. Inorganic deposits and organometallic drugs in tissue have been identified by the same localized ionization, which underscores that the defining object is the microprobe-sampled mass spectrum [4].