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机构地区:[1]广西大学轻工与食品工程学院,南宁市530004 [2]深圳职业技术学院应用化学与生物技术学院,深圳市518055 [3]广西大学动物科学与技术学院,南宁市530004
出 处:《中国药房》2010年第29期2760-2762,共3页China Pharmacy
基 金:广东省科技计划项目(粤科规划字[2009]159号)
摘 要:目的:建立测定降血压肽(AHP)/聚乳酸-羟基乙酸(PLGA)微球中AHP含量和包封率的反相高效液相色谱(RP-HPLC)法。方法:样品经二氯甲烷破坏并用水萃取后进行测定。反相色谱柱为Eclipse XDB-C18,流动相为乙腈-水(含0.05%三氟乙峰酸)均=得1到7∶很83好,流的速分为离1,.0A mHPL.检m测in浓-1,度柱线温性为范30围℃为,2检5~测6波25长μ为g.1m9L9-n(1mr,=进0样.99量9为9),2平0μ均L回。收结率果为:在9此8.7色8%谱,条日件内下和A日H间P与精辅密料度及分溶别为剂0.53%、0.86%(n=5)。结论:所建立的方法操作简单、快速,结果准确、可靠,可用于AHP/PLGA微球中主药含量及包封率的测定。OBJECTIVE: To establish RP-HPLC method for the content determination of AHP and encapsulation efficacy detection in AHP/PLGA microsphere.METHODS: The microspheres were dissolved by methylene dichloride,and the drug encapsulated in the microspheres could be extracted by water.The separation was performed on Eclipse XDB-C18 column with mobile phase consisted of acetonitrile-water(0.05%TFA)(17 ∶ 83) at flow rate of 1.0 mL·min^-1.The detection wavelength was set at 199 nm and column temperature was 30 ℃.Injection volume was 20 μL.RESULTS: AHP was well-separated from other components.The linear range of AHP was 25~625 μg·mL^-1(r=0.999 9) with an average recovery of 98.78%.The RSD of intra-day and inter-day were 0.53% and 0.86%(n=5).CONCLUSION: The method is simple,rapid,accurate and reliable for the content determination and encapsulation efficacy detection of AHP/PLGA microspheres.
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