[Fingerprint analysis of Luotong capsule by HPLC].Zhong Yao Cai. 2007 Apr; 30(4):460-3.ZY
Abstract
OBJECTIVE
To develop the chromatographic fingerprints of Luotong capsule by HPLC.
METHODS
The separation was performed on YMC-PacK ODS (4.6 mm x 250 mm, 5 microm) column with a mobile phase consisting of acetonitrile -0.5% phosphoric acid as gradient elution at the flow rate of 1.0 ml/min. The detective wavelength was 276 nm. The column temperature was 30 degrees C.
RESULTS
A standard HPLC fingerprint procedure was developed for Luotong capsule with 18 common peaks. The similarity of 10 batches of Luotong capsule was not lower than 0.978.
CONCLUSION
The mehtod is accurate, repeatable and useful for the quality control of Luotong capsule.
MeSH
Pub Type(s)
English Abstract
Journal Article
Research Support, Non-U.S. Gov't
Language
chi
PubMed ID
17674803
Citation
Zhao, Xiao-li, et al. "[Fingerprint Analysis of Luotong Capsule By HPLC]." Zhong Yao Cai = Zhongyaocai = Journal of Chinese Medicinal Materials, vol. 30, no. 4, 2007, pp. 460-3.
Zhao XL, Di LQ, Wu H, et al. [Fingerprint analysis of Luotong capsule by HPLC]. Zhong Yao Cai. 2007;30(4):460-3.
Zhao, X. L., Di, L. Q., Wu, H., & Li, W. D. (2007). [Fingerprint analysis of Luotong capsule by HPLC]. Zhong Yao Cai = Zhongyaocai = Journal of Chinese Medicinal Materials, 30(4), 460-3.
Zhao XL, et al. [Fingerprint Analysis of Luotong Capsule By HPLC]. Zhong Yao Cai. 2007;30(4):460-3. PubMed PMID: 17674803.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - [Fingerprint analysis of Luotong capsule by HPLC].
AU - Zhao,Xiao-li,
AU - Di,Liu-qing,
AU - Wu,Hao,
AU - Li,Wei-dong,
PY - 2007/8/7/pubmed
PY - 2008/10/31/medline
PY - 2007/8/7/entrez
SP - 460
EP - 3
JF - Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials
JO - Zhong Yao Cai
VL - 30
IS - 4
N2 - OBJECTIVE: To develop the chromatographic fingerprints of Luotong capsule by HPLC. METHODS: The separation was performed on YMC-PacK ODS (4.6 mm x 250 mm, 5 microm) column with a mobile phase consisting of acetonitrile -0.5% phosphoric acid as gradient elution at the flow rate of 1.0 ml/min. The detective wavelength was 276 nm. The column temperature was 30 degrees C. RESULTS: A standard HPLC fingerprint procedure was developed for Luotong capsule with 18 common peaks. The similarity of 10 batches of Luotong capsule was not lower than 0.978. CONCLUSION: The mehtod is accurate, repeatable and useful for the quality control of Luotong capsule.
SN - 1001-4454
UR - https://www.unboundmedicine.com/medline/citation/17674803/[Fingerprint_analysis_of_Luotong_capsule_by_HPLC]_
DB - PRIME
DP - Unbound Medicine
ER -