Injectable extracellular matrix hydrogel developed using porcine articular cartilage

被引:61
作者
Kwon, Jin Seon [1 ]
Yoon, So Mi [1 ]
Shim, Sun Woo [1 ]
Park, Ji Hoon [1 ]
Min, Kyung Jun [2 ]
Oh, Hyun Ju [1 ]
Kim, Jae Ho [1 ]
Kim, Young Jick [3 ]
Yoon, Jun Jin [4 ]
Choi, Byung Hyune [5 ]
Kim, Moon Suk [1 ]
机构
[1] Ajou Univ, Dept Mol Sci & Technol, Suwon 443749, South Korea
[2] Hongik Univ, Chem Engn & Mat Sci, Seoul 121791, South Korea
[3] Ajou Univ, Sch Med, Cell Therapy Ctr, Suwon 443759, South Korea
[4] RegenPrime Co Ltd, R&D Div, Suwon 442819, South Korea
[5] Inha Univ, Coll Med, Div Biomed & Bioengn Sci, Inchon 400103, South Korea
关键词
Porcine cartilage powder; Injectable; Hydrogel; BSA; Protein; BOVINE SERUM-ALBUMIN; IN-VIVO; DRUG-RELEASE; PHYSICOCHEMICAL PROPERTIES; BIOMEDICAL APPLICATIONS; PEPTIDE; ENCAPSULATION; DESIGN; ACID;
D O I
10.1016/j.ijpharm.2013.06.023
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
This work was first development of a delivery system capable of maintaining a sustained release of protein drugs at specific sites by using potentially biocompatible porcine articular cartilage. The prepared porcine articular cartilage powder (PCP) was easily soluble in phosphate-buffered saline. The PCP suspension easily entrapped bovine serum albumin-fluorescein isothiocyanate (BSA-FITC) in pharmaceutical formulations at room temperature. The aggregation of PCP and BSA-FITC was confirmed by dynamic light scattering. When the BSA-FITC-loaded PCP suspension was subcutaneously injected into rats, it gelled and formed an interconnecting three-dimensional PCP structure that allowed BSA to penetrate through it. The amount of BSA-FITC released from the PCP hydrogel was determined in rat plasma and monitored by real-time in vivo molecular imaging. The data indicated sustained release of BSA-FITC for 20 days in vivo. In addition, the PCP hydrogel induced a slight inflammatory response. In conclusion, we showed that the PCP hydrogel could serve as a minimally invasive therapeutics depot. (c) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:183 / 191
页数:9
相关论文
共 35 条
[1]
In Vivo Study of a Blended Hydrogel Composed of Pluronic F-127-Alginate-Hyaluronic Acid for its Cell Injection Application [J].
Abdi, Syed Izhar Haider ;
Choi, Jeong Yeon ;
Lee, Ji Seon ;
Lim, Hyun Ju ;
Lee, Changho ;
Kim, Jeehyun ;
Chung, Ho Yun ;
Lim, Jeong Ok .
TISSUE ENGINEERING AND REGENERATIVE MEDICINE, 2012, 9 (01) :1-9
[2]
Investigation of gelation mechanism of an injectable hydrogel based on chitosan by rheological measurements for a drug delivery application [J].
Aliaghaie, Marzieh ;
Mirzadeh, Hamid ;
Dashtimoghadam, Erfan ;
Taranejoo, Shahrouz .
SOFT MATTER, 2012, 8 (27) :7128-7137
[3]
Encapsulation of curcumin in self-assembling peptide hydrogels as injectable drug delivery vehicles [J].
Altunbas, Aysegul ;
Lee, Seung J. ;
Rajasekaran, Sigrid A. ;
Schneider, Joel P. ;
Pochan, Darrin J. .
BIOMATERIALS, 2011, 32 (25) :5906-5914
[4]
Amin S, 2009, SCI RES ESSAYS, V4, P1175
[5]
Proteins, polysaccharides, and their complexes used as stabilizers for emulsions: Alternatives to synthetic surfactants in the pharmaceutical field? [J].
Bouyer, Eleonore ;
Mekhloufi, Ghozlene ;
Rosilio, Veronique ;
Grossiord, Jean-Louis ;
Agnely, Florence .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2012, 436 (1-2) :359-378
[6]
The effect of protein structure on their controlled release from an injectable peptide hydrogel [J].
Branco, Monica C. ;
Pochan, Darrin J. ;
Wagner, Norman J. ;
Schneider, Joel P. .
BIOMATERIALS, 2010, 31 (36) :9527-9534
[7]
Biomedical applications of amino acid-modified chitosans: A review [J].
Casettari, Luca ;
Vllasaliu, Driton ;
Lam, Jenny K. W. ;
Soliman, Mahrrioud ;
Illum, Lisbeth .
BIOMATERIALS, 2012, 33 (30) :7565-7583
[8]
Transdermal delivery of selegiline from alginate-Pluronic composite thermogels [J].
Chen, Chih-Chieh ;
Fang, Chia-Lang ;
Al-Suwayeh, Saleh A. ;
Leu, Yann-Lii ;
Fang, Jia-You .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2011, 415 (1-2) :119-128
[9]
The chondrogenic differentiation of mesenchymal stem cells on an extracellular matrix scaffold derived from porcine chondrocytes [J].
Choi, Kyoung-Hwan ;
Choi, Byung Hyune ;
Park, So Ra ;
Kim, Byoung Ju ;
Min, Byoung-Hyun .
BIOMATERIALS, 2010, 31 (20) :5355-5365
[10]
Effect of drug physicochemical properties on swelling/deswelling kinetics and pulsatile drug release from thermoresponsive poly(N-isopropylacrylamide) hydrogels [J].
Coughlan, DC ;
Quilty, FP ;
Corrigan, OI .
JOURNAL OF CONTROLLED RELEASE, 2004, 98 (01) :97-114