A GC-FID Validated Method for the Quality Control of Eucalyptus globulus Raw Material and its Pharmaceutical Products, and GC-MS Fingerprinting of 12 Eucalyptus Species

被引:0
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作者
Bueno, Paula Carolina Pires [1 ]
Groppo Junior, Milton [2 ]
Bastos, Jairo Kenupp [1 ]
机构
[1] Univ Sao Paulo, Fac Pharmaceut Sci Ribeirao Preto, BR-14040903 Ribeirao Preto, SP, Brazil
[2] Univ Sao Paulo, Fac Philosophy Sci & Letters Ribeirao Preto, BR-14040901 Ribeirao Preto, SP, Brazil
关键词
1,8-Cineol; Capillary gas chromatography; Eucalyptus globulus; Method validation; Syrup; MEDICINES; EFFICACY; SAFETY;
D O I
暂无
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In this work we have validated a method to standardize and control the quality of Eucalyptus globulus raw material and phytomedicines containing either the essential oil or the fluid extract of this plant in the final formulation. Internal standardization provided a simple, fast, and reproducible GC-FID analytical method that accurately quantified 1,8-cineol in different E. globulus sub-products, such as its essential oil, dried leaves, fluid extract, and syrup. In addition, GC-MS identification of the main compounds of E. globulus species afforded fingerprints for the qualitative analysis of different Eucalyptus species.
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页码:1787 / 1790
页数:4
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