3.4. Leaves
Samara scientists have proposed a method for quan-
tifi cation of hawthorn blood-red leaves by differential
spectrophotometry at 412 nm in terms of hyperoside with
preliminary extraction of raw material with 70% ethyl
alcohol [47].
A procedure for quantifi cation of 2”-O-rhamno-
side-vitexin, vitexin, isovitexine, rutin and hyperoside in
hawthorn leaves is described by liquid chromatography
with ultraviolet detection [48].
There is also methods for quantifi cation of
2“-O-glucoside vitexin, 2”-O-rhamnoside vitexin, rutin
and hyperoside in hawthorn leaves by reversed-phase
high-performance liquid chromatography with ultravio-
let detection [49].
A group of Chinese scientists has quantifi ed ten com-
ponents: vitexin-2”-ramnoside, vitexin-glucoside, vitex-
in, hyperoside, isoquercitrine, chlorogenic acid, eucomic
acid, epicatechin, procyanidin B2 and C1 in the leaves of
Chinese hawthorn (Crataegus pinnatifi da Bge.) by meth-
od of high-performance liquid chromatography [50].
CONCLUSION. Thus, our analysis and system-
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