用UV-VIS对khemmometrics组合的光谱分析法验证了M. tomentosa花朵的存在

Samsul Hadi, Kunti Nastiti
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引用次数: 0

摘要

毛毛霉花具有多种活性,这些活性与铁皮毒霉花不同,但花朵相似,因此混合的风险很高。因此,本研究旨在利用紫外可见分光光度法与化学计量学相结合的方法防止混合物的发生。本研究采用的方法是将两种植物的提取物用甲醇p.a.溶解,在200-400 nm波长扫描光谱,数据采用偏最小二乘法分析。在对不同型号的白腰花进行鉴定时得到的结果,在248.14 ~ 222.5 nm扫描得到的数据RMSEC: 2.61, R2: 0.9971, RMSEP:5.78, R2: 0.9951, RMSECV:9.19, R2: 0.9655,在298.43 ~ 56.36nm扫描得到的数据RMSEC:0.929, R2: 0.9996, RMSEP:3.54, R2: 0.9956, RMSECV:10.5,R2:0.9591,通过对这两个数据的比较,选择RMSE最低值和R2最高值。本研究的结论是,在298.43 ~ 256.36nm波长范围内的二次衍生化是鉴定毛毛鼠的最佳模型。
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Autentikasi Bunga R.tomentosa dari Resiko Adulterasi M. Candidum dengan Metode Spektrofotometri UV-VIS Kombinasi Khemmometrik
R. tomentosa flowers have various activities and these activities are different from M. candidum flowers, but have similar flowers so the risk of mixing is very high. Therefore, this study aims to prevent the occurrence of mixtures using UV-VIS spectrophotometry method combined with chemometrics. The method used in this study was the extracts of the two species were dissolved with methanol p.a and scanned the spectra at a wavelength of 200-400 nm, data analysis using partial least squares. The results obtained in the authentication of Bunga R.tomentosa produced various models, at 248.14-222.5 nm scanning resulted in data RMSEC: 2.61, R2: 0.9971, RMSEP:5.78, R2: 0.9951 and RMSECV:9.19, R2: 0.9655, On scanning 298.43- 56.36nm produces data RMSEC:0.929, R2: 0.9996, RMSEP:3.54, R2: 0.9956 and RMSECV:10.5,R2:0.9591, by looking at the two data, the lowest RMSE value and the highest R2 value are selected. The conclusion in this study is that the best model for R.tomentosa authentication is the second derivatization with a wavelength of 298.43-256.36nm.
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