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高效液相色谱法测定新藤黄酸纳米粒中新藤黄酸的含量和包封率 被引量:3

Determination of Content and Entrapment Efficiency of Neo-gambogic Acid Nanoparticles by HPLC
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摘要 目的:建立新藤黄酸纳米粒中新藤黄酸含量和包封率的测定方法。方法:采用C18-ODS色谱柱(250mm×4.6mm,5μm),流动相为甲醇:1.0mol/L磷酸(9:1),流速为1.0ml/min,检测波长为360nm,进样容积为20μl,柱温为25℃。结果:新藤黄酸在10~120μg范围内线性关系良好,r=0.9999(n=7);新藤黄酸平均回收率为99.32%,RSD为1.03%(n=3)。平均含量为99.52%,包封率为83.81%.结论:高效液相色谱法准确、可靠、重复性好,可用于新藤黄酸纳米粒含量及其包封率的测定。 Objective: To establish a method for the determination of content and entrapment efficiency of neo-gambogie acid nanoparticles. Methods. Chromatographic conditions consisted of C18-columm, mobile phase (methanol: 1.0 mol/L H3PO4 :9: 1), LTV wavelength (360 nm), flow rate (1.0 ml/min) and column temperature (25℃). Results: Neo-gambogic acid showed a good linear relation with peak area at the range of 10-120μg , r : 0. 999 9 (n:7). The average recovery of neo-gambogic acid was 99.32%, RSD was 1.03% (n: 3). The average content of neo-gambogic acid was 99.52%. Entrapment efficiency was 83.81%. Conclusion: This method possesses advantages of accuracy, reliability and good reproducibility, and it can be used for the determination of content and entrapment efficiency of neo-gambogic acid nanoparticles.
出处 《安徽中医学院学报》 CAS 2009年第1期49-51,共3页 Journal of Anhui Traditional Chinese Medical College
关键词 新藤黄酸纳米粒 高效液相色谱法 含量测定 包封率 Neo-gambogic acid nanoparticles High performance liquid chromatography Content de- termination Entrapment efficiency
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参考文献10

  • 1吕归宝 杨秀贤 黄乔书.藤黄中新藤黄酸的分离及其结构.药学学报,1984,19(8):636-639.
  • 2曲宝玺,郝晓阁.藤黄Ⅱ号抗癌作用的实验研究[J].中国肿瘤临床,1991,18(1):50-52. 被引量:28
  • 3王效山.一种注射用新藤黄酸制剂及其制备方法、应用:中国,200510039059.2[P].2006-01-11.
  • 4吕归宝,方瑾.高效液相色谱法测定藤黄中藤黄酸与新藤黄酸含量[J].中草药,1988,19(7):10-12. 被引量:9
  • 5冯传平,周娟,黄鹏,马翔,刘修树,王效山.HPLC测定新藤黄酸的含量[J].安徽中医学院学报,2006,25(5):48-49. 被引量:6
  • 6张继芬,侯世祥,刘惠莲,王立,胡平,叶利民,王高森.葫芦素-聚乳酸纳米粒的制备及载药过程研究[J].中国中药杂志,2005,30(6):436-439. 被引量:10
  • 7Oommen E, Tiwari SB, Udupa N, et al. Niosome entrapped eyclodextrin methotrexate complex as a drug delivery system [J]. Ind J Pham, 1999, 31(4): 279-284.
  • 8HOU Dong zhi, XIE Chang sheng, HUANG Kai jin, et al. The production and characteristics of solid lipid nanoparticles[J]. Biomaterials, 2003, 24 (10) : 1781- 1785.
  • 9YL Su, ZY Fu, JY Zhang, et al. Microencapsulation of Radix salvia miltiorrhiza nanopartieles by spray-drying[J]. Powder Technology, 2008, 184 (1): 114-121.
  • 10Muller RH, Radtkem, Wissing SA. Nanostructured lipid matrices for improved microencapsulation of drugs [J] . Int J Pharm, 2002, 242(5) : 121-128.

二级参考文献18

  • 1Rodrigues J M, Croft S L, Fessi H, et al. Primaquine-loaded poly (lactide) nanoparticules: physicochemical study and acute tolerancein mice. Int J Pharm, 1995,126:253.
  • 2Santos N S, Magalhaes, Fessi H, et al. An in vitro release kinetic examinationand comparative evaluation between submicron emulsionand polylactic acid nanocapsules of clofibride. J Microencaps, 1995,12:195.
  • 3Marchais H, Benali S, Irache J M, et al. Entrapment efficiencyand initial release of phenylbutazone from nanocapsulesprepared from different polyesters. Drug Dev Ind Pharm, 1998, 24:883.
  • 4Cauchetier E, Deniau M, Fessi H, et al. Atovaquone-loaded nanocapsules: influence of the nature of the polymer on their in vitro characteristics. Int J Pharm, 2003, 50:273.
  • 5Paul M, Fessi H, Laatiris A, et al. Pentamidine-loaded poly(d,l-lactide) nanoparticles:physicochemical properties and stability work. Int J Pharm, 1997, 159:223.
  • 6Verger M L, Fluckiger L, Kim Y, et al. Preparation and characterization of nanoparticles containing an antihypertensive agent. Eur J Pharm, 1998,46:137.
  • 7.卫生部药品标准: 第十九册.[S].,1998.224.
  • 8吕归宝,杨秀贤,黄乔书.藤黄中新藤黄酸的分离及其结构[J]药学学报,1984(08).
  • 9孙瑞元.简捷实用的半数致死量综合计算法[J]药学学报,1963(02).
  • 10何林,蒋学华.阿克拉霉素A聚乳酸毫微粒的制备工艺研究[J].中国药学杂志,1998,33(5):289-291. 被引量:16

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