Characterization of structurally related adenovirus-laden silk-elastinlike hydrogels

被引:26
作者
Dandu, Ramesh [1 ]
Ghandehari, Hamidreza [1 ]
Cappello, Joseph [2 ]
机构
[1] Univ Maryland, Dept Pharmaceut Sci, Ctr Nanomed & Cellular Delivery, Baltimore, MD 21201 USA
[2] Prot Polymer Technol Inc, San Diego, CA USA
关键词
adenoviral gene delivery; controlled gene delivery; genetically engineered polymers; hydrogels; silk-elastinlike protein polymers; soluble fraction and swelling;
D O I
10.1177/0883911507085278
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Genetically engineered silk-elastinlike protein polymer (SELP) analogs, SELP-47K and -415 K, consisting of varying ratio(s) and length(s) of silk and elastin in their monomer repeats and capable of spontaneous hydrogel formation were evaluated as matrices for controlled adenoviral release in vitro. The degree of swelling (q) and the amount of soluble fraction of SELP hydrogel analogs were evaluated with and without the incorporation of adenoviruses. The results indicate that polymer concentration and structure and not the incorporated adenoviruses are the predominant factors that influence q and the soluble fraction in these hydrogels over a 28-day period. The release of adenoviruses was a function of polymer concentration and structure. The higher cumulative percentage release observed in SELP-415K compared to SELP-47K can be attributed to the longer elastin sequence in the polymer backbone. These results indicate the potential of customizing the network properties and release from SELPs by manipulating the macromolecular architecture using recombinant synthesis.
引用
收藏
页码:5 / 19
页数:15
相关论文
共 21 条
[1]   Poly(lactic-glycolic) acid copolymer encapsulation of recombinant adenovirus reduces immunogenicity in vivo [J].
Beer, SJ ;
Matthews, CB ;
Stein, CS ;
Ross, BD ;
Hilfinger, JM ;
Davidson, BL .
GENE THERAPY, 1998, 5 (06) :740-746
[2]   CORRELATION BETWEEN MESH SIZE AND EQUILIBRIUM DEGREE OF SWELLING OF POLYMERIC NETWORKS [J].
CANAL, T ;
PEPPAS, NA .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1989, 23 (10) :1183-1193
[3]   GENETIC-ENGINEERING OF STRUCTURAL PROTEIN POLYMERS [J].
CAPPELLO, J ;
CRISSMAN, J ;
DORMAN, M ;
MIKOLAJCZAK, M ;
TEXTOR, G ;
MARQUET, M ;
FERRARI, F .
BIOTECHNOLOGY PROGRESS, 1990, 6 (03) :198-202
[4]   In-situ self-assembling protein polymer gel systems for administration, delivery, and release of drugs [J].
Cappello, J ;
Crissman, JW ;
Crissman, M ;
Ferrari, FA ;
Textor, G ;
Wallis, O ;
Whitledge, JR ;
Zhou, X ;
Burman, D ;
Aukerman, L ;
Stedronsky, ER .
JOURNAL OF CONTROLLED RELEASE, 1998, 53 (1-3) :105-117
[5]  
DAVIDSON BL, 1997, ADV DRUG DELIV REV, V27, P59
[6]   Swelling behavior of a genetically engineered silk-elastinlike protein polymer hydrogel [J].
Dinerman, AA ;
Cappello, J ;
Ghandehari, H ;
Hoag, SW .
BIOMATERIALS, 2002, 23 (21) :4203-4210
[7]   Matrix immobilization enhances the tissue repair activity of growth factor gene therapy vectors [J].
Doukas, J ;
Chandler, LA ;
Gonzalez, AM ;
Gu, DL ;
Hoganson, DK ;
Ma, CL ;
Nguyen, T ;
Printz, MA ;
Nesbit, M ;
Herlyn, M ;
Crombleholme, TM ;
Aukerman, SL ;
Sosnowski, BA ;
Pierce, GF .
HUMAN GENE THERAPY, 2001, 12 (07) :783-798
[8]   Molecular engineering of silk-elastinlike polymers for matrix-mediated gene delivery: Biosynthesis and characterization [J].
Haider, Mohamed ;
Leung, Vivian ;
Ferrari, Franco ;
Crissman, John ;
Powell, James ;
Cappello, Joseph ;
Ghandehari, Hamidreza .
MOLECULAR PHARMACEUTICS, 2005, 2 (02) :139-150
[9]   Adenoviral gene delivery to solid tumors by recombinant silk-elastinlike protein polymers [J].
Hatefi, A. ;
Cappello, J. ;
Ghandehari, H. .
PHARMACEUTICAL RESEARCH, 2007, 24 (04) :773-779
[10]   Immunity to adenovirus and adeno-associated viral vectors: implications for gene therapy [J].
Jooss, K ;
Chirmule, N .
GENE THERAPY, 2003, 10 (11) :955-963