Similar words: cephalexin, icefall, duplexing, complexing, lexington, perplexing, multiplexing, alexia.
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1. The content of lincomycin hydrochloride and cefalexin in preparation were determined by HPLC. Results The manufacturing technique was feasible.
2. Methods:To eliminate the antimicrobial effect of Compound Cefalexin Capsules by recovery rate with 5 control trains.
3. Conclusion: The synthesis of Cefalexin by one step crystallization can greatly shorten the craft and lower the production cost.
4. Cefalexin descriptions can not say that the treatment of intestinal infections, eating it effective?
5. OBJECTIVE:To study the pharmacokinetics and bioavailability of cefalexin dispersible tablet in healthy male volunteers.
6. Objective To prepare lincomycin hydrochloride, cefalexin capsules andits standard for quality control.
7. Objective To prepare lincomycin hydrochloride, cefalexin capsules and establish its standard for quality control.
8. OBJECTIVE To investigate the influencing factors on release Compound Cefalexin sustained - release pellets in vitro.
9. Objective : To study the pharmacokinetics and bioavailability of cefalexin capsule.
10. Conclusion: The centrifugation and membrane filtration method should be suggested for Compound Cefalexin Capsules.
11. According to the drug sensitive test, Gbacillus was most sensitive to imipenem but its drug resistance to penicillin, cidomycin, cefalexin, clindamycin ect was more than 50%.
12. OBJECTIVE To investigate the influencing factors on release of Compound Cefalexin sustained-release pellets in vitro .
13. In accordance with the light absorbing property of stable suspension, the method for determinating the content of cefalexin capsule by new double wavelength spectrophotometry was established.
14. METHODS Single - factor method was used to investigate several factors affecting cefalexin release rate.
15. Objective:To establish the method of microbial limit for Compound Cefalexin Capsules.
16. The maximum application was cephalosporins antibiotics ; ranked the top three were cefixime capsule, injection cefmetazole sodium, sustained - release tablets cefalexin.
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17. Thermogravimetry was used to study the non-isothermal decomposition kinetics and the difference of stability between cefalexin and its excipients.
18. In this paper, the authors Adopt UV spectrophotometry to determine the content of. cefalexin and compare with the sutra iodimetry.
19. OBJECTIVE Near infrared diffuse reflectance spectrophotometry (NIRDRS) and chemometrics were applied to the quantitative analysis of cefalexin in capsules.
20. Similarity factor was used to evaluate the effect of all those influencing factors on release profiles of cefalexin .
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