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脂微球载药系统的研究进展

章秀丽,  马月琴,  李刚

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文章导航 > 药学实践与服务  > 2014 >  32(6): 409-411,459
章秀丽, 马月琴, 李刚. 脂微球载药系统的研究进展[J]. 药学实践与服务, 2014, 32(6): 409-411,459. doi: 10.3969/j.issn.1006-0111.2014.06.003
引用本文: 章秀丽, 马月琴, 李刚. 脂微球载药系统的研究进展[J]. 药学实践与服务, 2014, 32(6): 409-411,459. doi: 10.3969/j.issn.1006-0111.2014.06.003
shu
ZHANG Xiuli, MA Yueqin, LI Gang. Research development of lipid microsphere delivery system[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(6): 409-411,459. doi: 10.3969/j.issn.1006-0111.2014.06.003
Citation: ZHANG Xiuli, MA Yueqin, LI Gang. Research development of lipid microsphere delivery system[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(6): 409-411,459. doi: 10.3969/j.issn.1006-0111.2014.06.003
shu

脂微球载药系统的研究进展

doi: 10.3969/j.issn.1006-0111.2014.06.003

  • 解放军94医院药械科, 江西 南昌 330002

基金项目: 江西省自然科学基金项目(20122BAB215038).

Research development of lipid microsphere delivery system

  • Department of Pharmacy, No. 94 Hospital of PLA, Nanchang 330002, China

  • 摘要: 脂微球递药系统是药剂学研究的热点,从脂微球载药系统的形成机制、构建方法及关键影响因素等方面进行综述,介绍该领域研究的进展和一些新发现,以促进脂微球作为药物载体的开发和应用。
    Abstract: Lipid microsphere drug delivery system is a hot issue in pharmceutics studies. In this paper, the mechanism, preparation method and the key influence factors of lipid microsphere drug delivery system were reviewed respectively. Some new discovery and development were introduced in order to enhance the development and application of lipid microsphere drug delivery system as a drug delivery tool.
  • [1] Liu ZZ, Feng YY, Zhang LL, et al. Pharmacokinetics and tissue distribution of larotaxel in rats: comparison of larotaxel-loaded microsphere with larotaxel-solution[J]. Cancer Chemother Pharmacol, 2013, 71(5): 1131-1139.
    [2] McClements DJ. Advances in fabrication of emulsions with enhanced functionality using structural design principles[J]. Curr Opin Colloid Interf Sci, 2012, 17(5): 235-245.
    [3] Groves MJ. The redistribution of bulk aqueous phase phospholipids during thermal stressing of phospholipid-stabilized emulsions[J]. Pharm Pharmacol, 1993, 45(7): 592.
    [4] Morais JM, Burgess DJ. Long acting injections and implants: micro-and nano-emulsions (controlled release parenteral drug delivery systems)[M].London: Springer, 2012: 221-238.
    [5] Yue PF, Lu XY, Liao MX, et al. The effect of oil components and homogenization conditions on the physicochemical properties of zedoary turmeric oil submicron emulsions[J]. J Dispers Sci Technol, 2010, 31(11):1535-1540.
    [6] Patel R, Joshi J. An overview on nanoemulsion: a novel approach[J]. Int J Pharml Sci Res, 2012, 3(12): 4640-4650.
    [7] Bague S, Philips B, Rabinovich-Guilatt L, et al. Ophthalmic oil-in-water type emulsion with stable zeta potential[P].USA WO2006050838 A2, 2005-10-10.
    [8] Akkar A, Muller RH. Intravenous itraconazole emulsions produced by SolEmuls technology[J]. Eur J Pharm Biopharm, 2003, 56(1): 29-36.
    [9] Müller RH, Schmidt S, Buttle I, et al. SolEmuls®-novel technology for the formulation of i.v. emulsions with poorly soluble drugs[J]. Int J Pharm, 2004, 269(2): 293-302.
    [10] Yue PF, Li FQ, Liao MX, et al. Process optimization, characterization, and release study in vitro of an intravenous puerarin lipid micropheres loaded with the phospholipid complex[J]. J Dispers Sci Technol, 2011, 32(1): 1-10.
    [11] Yue PF, Zheng Q, Wu B, et al. Application of plackett-burman design and box-behnken design to achieve process optimization for geniposide submicron emulsion[J]. J Dispers Sci Technol, 2012, 33(2): 213-222.
    [12] Ma YQ, Li G, Xu JH, et al. Combination of submicroemulsion and phospholipid complex for novel delivery of ursodeoxycholic acid[J]. Pharm Dev Technol,2014,19(3):363-372.
    [13] Gulati Neha, Gupta Himanshu. Parenteral drug delivery: a review[J]. Recent Patent Drug Deliv Form, 2011, 5(2): 133-145.
    [14] Yamamura K, Nakao M, Yano K, et al. Stability of forskolin in lipid emulsions and oil/water partition coefficients[J]. Chem Pharm Bull,1991, 39(4):1032-1034.
    [15] Bhalerao AV, Singh SS. In situ gelling ophthalmic drug delivery system for glaucoma[J]. Int J Pharm Biosci, 2011, 2(2): 7-14.
    [16] Patel Y, Poddar A, Sawant K. Formulation and characterization of Cefuroxime Axetil nanoemulsion for improved bioavailability[J]. J Pharm Bioallied Sci, 2012, 4(1): S4-S5.
    [17] Ammar H, Salama H, Ghorab M, et al. Nanoemulsion as a potential ophthalmic drug delivery system for Dorzolamide hydrochloride[J]. AAPS Pharm Sci Tech, 2009, 10(3): 808-819.
    [18] Gan L, Wang J, Jiang M, et al.Recent advances in topical ophthalmic drug delivery with lipid-based nanocarriers[J]. Drug Discov Today, 2013, 18(5-6): 290-297.
    [19] Lu Y, Qi J, Wu W. Absorption, disposition and pharmacokinetics of nanoemulsions[J]. Curr Drug Metab,2012, 13(4): 418-428.
    [20] Sultana Y, Maurya DP, Iqbal Z,et al. Nanotechnology in ocular delivery: current and future directions[J]. Drugs Today, 2011, 47(6): 441-455.
    [21] Zhang N, Zhang Q, Chu T, et al. Formulation optimization of prostaglandin E1-loaded lipid emulsion: enhanced stability and reduced biodegradation[J]. Pharm Dev Tech, 2013, 18(4): 804-812.
    [22] GaoY, Xu PF, Chen LL, Li YP. Prostaglandin E1 encapsulated into lipid nanoparticles improves its anti-inflammatory effect with low side-effect[J]. Int J Pharm, 2010, 387(1-2): 263-271.
    [23] Ueki R, Tanimoto M, Tatara T, et al. Emulsion of flurbiprofen axetil reduces propofol injection pain due to a decrease in free propofol concentration[J]. J Anesth, 2007, 21 (3): 325-329.
    [24] Shen J, Gan L, Zhu C, et al. Novel NSAIDs ophthalmic formulation: flurbiprofen axetil emulsion with low irritancy and improved anti-inflammation effect[J]. Int J Pharm, 2011, 412(1-2):115-122.
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出版历程
  • 收稿日期:  2013-05-21
  • 修回日期:  2014-03-17

脂微球载药系统的研究进展

doi: 10.3969/j.issn.1006-0111.2014.06.003
  • 解放军94医院药械科, 江西 南昌 330002
    • 基金项目:  江西省自然科学基金项目(20122BAB215038).
  • 收稿日期: 2013-05-21
  • 修回日期: 2014-03-17

摘要: 脂微球递药系统是药剂学研究的热点,从脂微球载药系统的形成机制、构建方法及关键影响因素等方面进行综述,介绍该领域研究的进展和一些新发现,以促进脂微球作为药物载体的开发和应用。

English Abstract

章秀丽, 马月琴, 李刚. 脂微球载药系统的研究进展[J]. 药学实践与服务, 2014, 32(6): 409-411,459. doi: 10.3969/j.issn.1006-0111.2014.06.003
引用本文: 章秀丽, 马月琴, 李刚. 脂微球载药系统的研究进展[J]. 药学实践与服务, 2014, 32(6): 409-411,459. doi: 10.3969/j.issn.1006-0111.2014.06.003
shu
ZHANG Xiuli, MA Yueqin, LI Gang. Research development of lipid microsphere delivery system[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(6): 409-411,459. doi: 10.3969/j.issn.1006-0111.2014.06.003
Citation: ZHANG Xiuli, MA Yueqin, LI Gang. Research development of lipid microsphere delivery system[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(6): 409-411,459. doi: 10.3969/j.issn.1006-0111.2014.06.003
shu

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