Compression profiles of different molecular weight chitosans

被引:19
作者
Alakayleh, Faisal [1 ]
Rashid, Iyad [2 ]
Al-Omari, Mahmoud M. H. [2 ]
Al-Sou'od, Khaldoun [3 ]
Chowdhry, Babur Z. [4 ]
Badwan, Adnan A. [2 ]
机构
[1] Petra Univ, Dept Pharmaceut & Pharmaceut Technol, Coll Pharm, Amman, Jordan
[2] Jordanian Pharmaceut Mfg Co, Naur, Jordan
[3] Al Albait Univ, Dept Chem, Irbid, Jordan
[4] Univ Greenwich, Fac Sci & Engn, Medway Campus, Chatham, Kent, England
关键词
Chitosan; Molecular weight; Compression force; Molecular modeling; DRUG-RELEASE; COMPACTION BEHAVIOR; POWDER COMPACTION; EXTENDED-RELEASE; TABLET STRENGTH; MATRIX TABLETS; DELIVERY; NANOPARTICLES; PARAMETERS; DEPOLYMERIZATION;
D O I
10.1016/j.powtec.2016.05.019
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The compression behavior of hydrophilic chitosan has been investigated as a function of molecular weight (MW), ranging from 8 to 100 kDa. Powder packing, plasticity, elasticity, brittle-fracture nature were evaluated using force displacement curves and Heckel/Kawakita analysis upon compression of different MW chitosan powders. The compacts produced were subjected to ejection work determination and tensile strengths analysis, the later using Leuenberger equation. Molecular modeling was used to correlate the MW-binding energy dependence on the physical strength of the chitosan compacts. The high work of compression of the low MW (<= 30 kDa) chitosans is accounted for their brittle nature upon compression. At high compression forces (>3 kN), the low MW chitosan compacts exhibited slightly lower tensile strength due to their increasing extents of elastic recovery and ejection work. Lower particle size of chitosan enhances lower fragmentation, packing, and frictional tendency that can be related to an increase in plastic deformation and compacts tensile strength. In molecular modeling, the calculated higher binding energies of the high MW chitosan (88 kDa) than that of the low MW chitosan (8 kDa) may further explain its rigid, complex nature when compared to low MW chitosan. Upon compression, increasing MW of chitosan is manifested as higher energies for densification which in turn determines the extent of helical packing from intermingled molecular to open structure as the MW is decreased. Such changes in structural configuration are suggested to contribute to the transfer from plastic to brittle-fracture nature with high packing extent of chitosan upon compression when the MW is reduced. The foregoing may justify the slow diclofenac Na drug release upon dissolution testing when low MW chitosan is used in tablet preparation. (C) 2016 Published by Elsevier B.V.
引用
收藏
页码:107 / 118
页数:12
相关论文
共 68 条
[1]   Branched chitosans: Effects of branching parameters on rheological and mechanical properties [J].
Aggarwal, Dinesh ;
Matthew, Howard W. T. .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2007, 82A (01) :201-212
[2]   Formulation and In vitro assessment of sustained release terbutaline sulfate tablet made from binary hydrophilic polymer mixtures [J].
Al-Akayleh, Faisal ;
Al Remawi, Mayyas ;
Rashid, Iyad ;
Badwan, Adnan .
PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2013, 18 (05) :1204-1212
[3]   Hyaluronic acid-coated chitosan nanoparticles: Molecular weight-dependent effects on morphology and hyaluronic acid presentation [J].
Almalik, Abdulaziz ;
Donno, Roberto ;
Cadman, Christopher J. ;
Cellesi, Francesco ;
Day, Philip J. ;
Tirelli, Nicola .
JOURNAL OF CONTROLLED RELEASE, 2013, 172 (03) :1142-1150
[4]  
[Anonymous], 2007, BRIT PHARMACOPOEIA B, VI, P456
[5]   PERCOLATION THEORY AND COMPACTIBILITY OF BINARY POWDER SYSTEMS [J].
BLATTNER, D ;
KOLB, M ;
LEUENBERGER, H .
PHARMACEUTICAL RESEARCH, 1990, 7 (02) :113-117
[6]   Spray-Dried Chitosan as a Direct Compression Tableting Excipient [J].
Chinta, Dakshinamurthy Devanga ;
Graves, Richard A. ;
Pamujula, Sarala ;
Praetorius, Natalie ;
Bostanian, Levon A. ;
Mandal, Tarun K. .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2009, 35 (01) :43-48
[7]  
de Blaey C J, 1970, Pharm Weekbl, V105, P241
[8]   Preparation and characterization of drug-loaded chitosan-tripolyphosphate microspheres by spray drying [J].
Desai, KGH ;
Park, HJ .
DRUG DEVELOPMENT RESEARCH, 2005, 64 (02) :114-128
[9]   Synthesis and characterization of cross-linked chitosan microspheres for drug delivery applications [J].
Dini, E ;
Alexandridou, S ;
Kiparissides, C .
JOURNAL OF MICROENCAPSULATION, 2003, 20 (03) :375-385
[10]   Bioadhesive Controlled Metronidazole Release Matrix Based on Chitosan and Xanthan Gum [J].
Eftaiha, Ala'a F. ;
Qinna, Nidal ;
Rashid, Iyad S. ;
Al Remawi, Mayyas M. ;
Al Shami, Munther R. ;
Arafat, Tawfiq A. ;
Badwan, Adnan A. .
MARINE DRUGS, 2010, 8 (05) :1716-1730