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左旋多巴甲酯在PLGA微球的稳定性研究

Stability of Levodopa Methyl Ester-loaded PLGA Microspheres
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摘要 目的:考察左旋多巴甲酯在PLGA微球中的稳定性并探讨其稳定方法。方法:利用HPLC的方法考察了左旋多巴甲酯在不同pH值和光照的环境中和微球里的稳定性。结果:左旋多巴甲酯在pH 3中稳定,在微球中也可以稳定一周。结论:包封左旋多巴甲酯在PLGA微球中,是一种有效地保护了左旋多巴甲酯在微球中的活性,可以实现长效缓释,是一种可行的方案。 Objective: To develop an effective method and analysis of stability levodopa methyl ester. Methods: Stability of levodopa methyl ester in different pH, illumination and in PLGA microspheres were analyzed by HPLC method. Results: Levodopa methyl ester can be stabilized at pH 3 and in PLGA microspheres for 1 week. Conclusion: The preparation of PLGA microspheres of levodopa methyl ester through the encapsulation method can protect the bioactivity of the levodopa methyl ester in the microspheres. This method is an effective technique for levodopa methyl ester sustained release.
出处 《现代生物医学进展》 CAS 2013年第24期4605-4607,共3页 Progress in Modern Biomedicine
基金 国家自然科学基金项目(81173001) 上海科委纳米专项(11nm0503300)
关键词 左旋多巴甲酯 稳定性 微球 Levodopa methyl ester Stability Microsphere
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参考文献18

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二级参考文献39

  • 1周青,张世忠,徐如祥.帕金森病的治疗现状和展望[J].中国临床康复,2004,8(16):3102-3103. 被引量:3
  • 2Sherer TB, Betarbet R, Greenamyre JT. Pathogenesis of Parkinson's disease[J]. Curt Opin Investig Drugs, 2001,2(5):657-662.
  • 3Andres M, Iozano, Suneil K, Kalia. New Movement in Pakinson's [J]. Science, 2005,6:58-65.
  • 4Eskow KL, Dupre KB, Barnum CJ, et al. The role of the dorsal raphe nucleus in the development, expression, and treatment of L-dopa-in- duced dyskinesia in hemiparkinsonian rats [J]. Synapse, 2009, 63(7): 610-620.
  • 5Aubert I, Guigoni C, Li Q, et al. Enhanced preproenkephalin-B-de- rived opioid transmission in striatum and subthalamic nucleus con- verges upon globus pallidus intemalis in L-3,4-dihydroxypheny!ala- nine-induced dyskinesia[J]. Biol Psychiatry, 2007, 61(7):836-844.
  • 6Bishop C, Taylor JL, Kuhn DM, et al. MDMA and fenfluramine reduce L-DOPA-induced dyskinesia via indirect 5-HTIA receptor stimulation[J]. Eur J Neurosci, 2006, 23(10):2669-2676.
  • 7Jaunarajs KL, Dupre KB, Steiniger A, et al. Serotonin 1B receptor stimulation reduces D1 receptor agonist-induced dyskinesia [J]. Neu- roreport, 2009, 20(14): 1265-1269.
  • 8Carta M, Carlsson T, Kirik D, et al. Dopamine released from 5-HT ter- minals is the cause of L-DOPA-indueed dyskinesia in parkinsonian rats[J]. Brain, 2007,130(Pt 7): 1819-1833.
  • 9Meissner W, Ravenseroft P, Reese R, et al. Increased slow oscillatory activity in substantia nigra pars reticulata triggers abnormal involun- tary movements in the 6-OHDA-lesioned rat in the presence of exces- sive extracellular striatal dopamine [J]. Neurobiol Dis, 2006, 22(3): 586-598.
  • 10Morissette M, Dridi M, Calon F, et al. Prevention of levodopa-in- duced dyskinesias by a selective NRIA/2B N-methyl-D-aspartate receptor antagonist in parkinsonian monkeys: implication of pre- proenkephalin[J]. Mov Disord, 2006, 21 (1):9-17.

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