Preparation and Characterization of Succinyl-Chitosan Nanoparticles for Drug Delivery

被引:16
作者
Monsalve, Yuliana [1 ]
Sierra, Ligia [1 ]
Lopez, Betty L. [1 ]
机构
[1] Univ Antioquia, Fac Exact & Nat Sci, Inst Chem, Sci Mat Res Grp, St 70 52-21, Medellin, Colombia
关键词
biodegradable; drug delivery systems; nanoparticles; polymer; succinyl-chitosan;
D O I
10.1002/masy.201400128
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Succinyl-Chitosan (SCS), a water soluble CS derivative, exhibits biocompatibility, low toxicity and long-term retention in the body. SCS offers unique characteristics as polymer for obtaining drug delivery nanosystems, due to its many reactive amino, hydroxyl, and carboxylic acid pendant groups. Chemical modifications of SCS with antibodies and other active species are easily achieved through bonding with these groups, allowing targeting and detection. In this work, SCS was obtained by amidation of primary amine groups of CS with succinic anhydride. The succinylation degree, determined by H-1-NMR, was 28%. Evaluation by zeta potential measurements of SCS showed a pH-dependent charge profile, which can be conveniently exploited to prepare pH-sensitive nanoparticles. Colloidal stable SCS/CS and SCS nanoparticles, useful in drug delivery, were prepared by ionic crosslinking from mixtures of CS and SCS in different weight percentages. Nanoparticles with sizes between 140-250 nm (after purification process) are obtained, which through further surface functionalization are suitable for application in drug delivery. The colloidal stability of the particles in water was studied by particle size measurements during 30 days and aggregation or formation of larger particles was not observed.
引用
收藏
页码:91 / 98
页数:8
相关论文
共 21 条
  • [1] Challenges in evaluation of chitosan and trimethylated chitosan (TMC) as mucosal permeation enhancers: From synthesis to in vitro application
    Benediktsdottir, Berglind Eva
    Baldursson, Olafur
    Masson, Mar
    [J]. JOURNAL OF CONTROLLED RELEASE, 2014, 173 : 18 - 31
  • [2] Studies on effect of pH on cross-linking of chitosan with sodium tripolyphosphate: A technical note
    Bhumkar, Devika R.
    Pokharkar, Varsha B.
    [J]. AAPS PHARMSCITECH, 2006, 7 (02)
  • [3] Calvo P, 1997, J APPL POLYM SCI, V63, P125, DOI 10.1002/(SICI)1097-4628(19970103)63:1<125::AID-APP13>3.0.CO
  • [4] 2-4
  • [5] Formation mechanism of monodisperse, low molecular weight chitosan nanoparticles by ionic gelation technique
    Fan, Wen
    Yan, Wei
    Xu, Zushun
    Ni, Hong
    [J]. COLLOIDS AND SURFACES B-BIOINTERFACES, 2012, 90 : 21 - 27
  • [6] Evaluation of N-succinyl-chitosan as a systemic long-circulating polymer
    Kato, Y
    Onishi, H
    Machida, Y
    [J]. BIOMATERIALS, 2000, 21 (15) : 1579 - 1585
  • [7] Biodegradation, biodistribution and toxicity of chitosan
    Kean, T.
    Thanou, M.
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2010, 62 (01) : 3 - 11
  • [8] Extraction of chitin from prawn shells and conversion to low molecular mass chitosan
    Mohammed, Musarrat H.
    Williams, Peter A.
    Tverezovskaya, Olga
    [J]. FOOD HYDROCOLLOIDS, 2013, 31 (02) : 166 - 171
  • [9] A novel permeation enhancer: N-succinyl chitosan on the intranasal absorption of isosorbide dinitrate in rats
    Na, Lidong
    Wang, Juan
    Wang, Linlin
    Mao, Shirui
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2013, 48 (1-2) : 301 - 306
  • [10] Targeted delivery of low molecular drugs using chitosan and its derivatives
    Park, Jae Hyung
    Saravanakumar, Gurusamy
    Kim, Kwangmeyung
    Kwon, Ick Chan
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2010, 62 (01) : 28 - 41