去唾液酸糖蛋白受体介导的肝靶向脂质体配体的酶促催化合成研究

郭波红 程怡 林绿萍 吴卫 林德晖

中国药学杂志 ›› 2012, Vol. 47 ›› Issue (1) : 40-43.

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中国药学杂志 ›› 2012, Vol. 47 ›› Issue (1) : 40-43.
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去唾液酸糖蛋白受体介导的肝靶向脂质体配体的酶促催化合成研究

  • 郭波红,程怡,林绿萍,吴卫,林德晖
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Study on the Enzyme-Catalyzed Synthesis of Ligands for ASGPR-mediated Liver Targeting Liposomes

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摘要

目的 用酶促催化乳糖酸与十八胺合成一种可用于镶嵌脂质体表面的去唾液酸糖蛋白靶向配体修饰物。方法 通过红外光谱(IR)、质谱(ESI-MS)和核磁共振(H-NMR)对产物结构进行确证,并对酶种类、反应介质、酶的加入量、底物摩尔比、反应温度等影响因素进行考察。结果 二甲基亚砜作为反应介质;Novozym 435固定化脂肪酶作为催化剂、酶加入量为400 U·mL、乳糖酸和十八胺的摩尔比为2∶1、40 ℃下反应24 h,十八胺的转化率可达99%以上。结论 酶促催化法可用来合成肝靶向脂质体配体。

Abstract

OBJECTIVE To synthesize asialoglycoprotein receptor ligand-targeted modifier which is used to insert the surface of liposome by enzyme-catalyzed amidation of lactobionic acid and stearamine. METHODS The structure of the product was confirmed by IR, ESI-MS and H-NMR. The effects of types and quantity of enzyme, organic solvents, molar ratio of substrate and temperature of reaction were studied. RESULTS When using DMSO as reaction medium, Novozym 435 immobilized lipase at 400 U·mL, molar ratio of lactobionic acid to stearamine at 2∶1, and reacting at 40 ℃ for 24 h, the transformation of stearamine reached more than 99%. CONCLUSION The enzyme catalysis is useful for synthesizing liver targeting liposomes.

关键词

酶促催化 / 去唾液酸糖蛋白受体 / 配体 / 十八胺

Key words

enzyme-catalyzed / asialoglycoprotein receptor / ligand / stearamine

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郭波红 程怡 林绿萍 吴卫 林德晖. 去唾液酸糖蛋白受体介导的肝靶向脂质体配体的酶促催化合成研究[J]. 中国药学杂志, 2012, 47(1): 40-43
Study on the Enzyme-Catalyzed Synthesis of Ligands for ASGPR-mediated Liver Targeting Liposomes[J]. Chinese Pharmaceutical Journal, 2012, 47(1): 40-43

参考文献


[1] FALLON R J, SCHWARTZ A L. Receptor-mediated delivery of drugs to hepatocytes [J]. Adv Drug Deliv Rev, 1989, 4(2): 49-63.
[2] DONATI I, GAMINI A, VETERE A, et al. Synthesis, characterization,and preliminary biological study of glycoconjugates of poly(styrene-co-maleicacid) [J]. Biomacromolecules, 2002, 3(4): 805-812.
[3] WU J, NANTZ M H, ZERN M A. Targeting hepatocytes for drug and gene delivery: emerging novel approaches and application [J]. Front Biosci, 2002, 7(3):d717-725.
[4] STOCKERT R J. The asialoglyeoprotein receptors: relationships between strueture,function,and expression [J]. Physiol Rev, 1995, 75(3): 591-593.
[5] WANG S N, DENG Y H, XU H, et al. Synthesis of a novel galactosylated lipid and its application to the hepatocyte-selective targeting of liposomal doxorubicin[J]. Eur J Pharm Biopharm, 2006, 62(1):32-38.
[6] LU J,SUN X,HAI L, et al. Liver targeting of galactosylated liposome-polycation-DNA complexes[J]. West China J Pharm Sci(华西药学杂志), 2007, 22(3): 239-241.
[7] KIM C K, MIN K H, OH Y K, et al. Preparation and lectin binding characteristics of N-stearyl lactobionamide liposomes[J]. Int J Pharm, 1996, 128(1-2): 65-71.
[8] LEE M Y, DORDICK J S. Enzyme activation for nonaqueous media [J]. Curr Opin Biotech, 2002, 13 (4): 376-384.
[9] WU C Y, LI C X. Determination of octadecane amine by gas chromatography [J]. Synthetic Lubricants(合成润滑材料), 2005, 32(3): 12-14.

基金

国家自然科学基金资助项目(30772790);广东省自然科学基金资助项目(S2011040003133)
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