Chitosan nanoparticles/cellulose nanocrystals nanocomposites as a carrier system for the controlled release of repaglinide

被引:59
作者
Abo-Elseoud, Wafaa S. [1 ,2 ]
Hassan, Mohammad L. [1 ,2 ,3 ]
Sabaa, Magdy W. [4 ]
Basha, Mona [5 ]
Hassan, Enas A. [1 ,2 ]
Fadel, Shaimaa M. [1 ,2 ]
机构
[1] Natl Res Ctr, Ctr Excellence Adv Sci, Cellulose & Paper Dept, Giza 12622, Egypt
[2] Natl Res Ctr, Ctr Excellence Adv Sci, Adv Mat & Nanotechnol Grp, Giza 12622, Egypt
[3] Cairo Univ, Egypt Nanotechnol Ctr, 6Th October City 12588, Egypt
[4] Cairo Univ, Fac Sci, Chem Dept, Giza 12613, Egypt
[5] Natl Res Ctr, Pharmaceut Technol Dept, Cairo 12622, Egypt
关键词
Cellulose nanocrystals; Palm fruit stalks; Chitosan nanoparticles; Repaglinide; Controlled release; IN-VIVO EVALUATION; DRUG-DELIVERY; CELLULOSE NANOCRYSTALS; VITRO; DISSOLUTION; MICROPARTICLES; OPTIMIZATION;
D O I
10.1016/j.ijbiomac.2018.01.044
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The aim of the present work was to study the use of cellulose nanocrystals (CNC) and chitosan nanoparticles (CHNP) for developing controlled-release drug delivery system of the anti-hyperglycemic drug Repaglinide (RPG). CNC was isolated from palm fruit stalks by sulfuric acid hydrolysis; the dimensions of the isolated nanocrystals were 86-237 nm in length and 5-7 nm in width. Simple and economic method was used for the fabrication of controlled release drug delivery system from CNC and CHNP loaded with RPG drug via ionic gelation of chitosan in the presence of CNC and RPG. The prepared systems showed high drug encapsulation efficiency of about similar to 98%. Chemical modification of CNC by oxidation to introduce carboxylic groups on their surface (OXCNC) was also carried out for further controlling of RPG release. Particles size analysis showed that the average size of CHNP was about 197 nm while CHNP/CNC/RPG or CHNP/OXCNC/RPG nanoparticles showed average size of 215-310 nm. Compatibility studies by Fourier transform infrared (FTIR) spectroscopy showed no chemical reaction between RPG and the system's components used. By studying the drug release kinetic, all the prepared RPG formulations followed Higuchi model, indicating that the drug released by diffusion through the nanoparticles polymeric matrix. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:604 / 613
页数:10
相关论文
共 52 条
[1]   A new self-emulsifying drug delivery system (SEDDS) for poorly soluble drugs: Characterization, dissolution, in vitro digestion and incorporation into solid pellets [J].
Abdalla, Ahmed ;
Klein, Sandra ;
Maedder, Karsten .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2008, 35 (05) :457-464
[2]   Use of Cellulose and Oxidized Cellulose Nanocrystals from Olive Stones in Chitosan Bionanocomposites [J].
Abou-Zeid, Ragab E. ;
Hassan, Enas A. ;
Bettaieb, Fedia ;
Khiari, Ramzi ;
Hassan, Mohammad L. .
JOURNAL OF NANOMATERIALS, 2015, 2015
[3]  
Adam Z., 2007, Jurnal Sains Kesihatan Malaysia, V5, P9
[4]   Comparative release studies of two cationic model drugs from different cellulose nanocrystal derivatives [J].
Akhlaghi, Seyedeh Parinaz ;
Tiong, Daryl ;
Berry, Richard M. ;
Tam, Kam Chiu .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2014, 88 (01) :207-215
[5]  
[Anonymous], 1967, Methods of wood chemistry
[6]   An injectable drug delivery platform for sustained combination therapy [J].
Baumann, M. Douglas ;
Kang, Catherine E. ;
Stanwick, Jason C. ;
Wang, Yuanfei ;
Kim, Howard ;
Lapitsky, Yakov ;
Shoichet, Molly S. .
JOURNAL OF CONTROLLED RELEASE, 2009, 138 (03) :205-213
[7]   Studies on effect of pH on cross-linking of chitosan with sodium tripolyphosphate: A technical note [J].
Bhumkar, Devika R. ;
Pokharkar, Varsha B. .
AAPS PHARMSCITECH, 2006, 7 (02)
[8]   Chitosan and chitosan ethylene oxide propylene oxide block copolymer nanoparticles as novel carriers for proteins and vaccines [J].
Calvo, P ;
RemunanLopez, C ;
VilaJato, JL ;
Alonso, MJ .
PHARMACEUTICAL RESEARCH, 1997, 14 (10) :1431-1436
[9]   Modeling and comparison of dissolution profiles [J].
Costa, P ;
Manuel, J ;
Lobo, S .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 13 (02) :123-133
[10]   Preparation and in vivo evaluation of mucoadhesive microparticles containing amoxycillin-resin complexes for drug delivery to the gastric mucosa [J].
Cuña, M ;
Alonso, MJ ;
Torres, D .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2001, 51 (03) :199-205