In situ gelling silk-elastinlike protein polymer for transarterial chemoembolization

被引:57
作者
Poursaid, Azadeh [1 ,3 ]
Price, Robert [2 ,3 ]
Tiede, Andrea [1 ]
Olson, Erik [1 ]
Huo, Eugene [4 ]
McGill, Lawrence [5 ]
Ghandehari, Hamidreza [1 ,2 ,3 ]
Cappello, Joseph [2 ]
机构
[1] Univ Utah, Dept Bioengn, Salt Lake City, UT 84112 USA
[2] Univ Utah, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT 84112 USA
[3] Univ Utah, Nano Inst Utah, Utah Ctr Nanomed, Salt Lake City, UT 84112 USA
[4] Vet Affairs Hosp, Salt Lake City, UT 84108 USA
[5] Associated Reg & Univ Pathologists, Salt Lake City, UT 84107 USA
关键词
Embolization; TACE; Recombinant polymers; Hepatocellular carcinoma; HEPATOCELLULAR-CARCINOMA; BIOMIMETIC DESIGN; DRUG-DELIVERY; TRENDS;
D O I
10.1016/j.biomaterials.2015.04.015
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Hepatocellular carcinoma annually affects over 700,000 people worldwide and trends indicate increasing prevalence. Patients ineligible for surgery undergo loco-regional treatments such as transarterial chemoembolization (TACE) to selectively target tumoral blood supply. Using a microcatheter, chemotherapeutics are infused followed by an embolic agent, or the drug is encapsulated by the embolic moiety; simultaneously inducing stasis while delivering localized chemotherapy.,Presently, several products are used, but no universally accepted system is promoted because very disparate limitations exist. The goal of this investigation was to design and develop in situ gelling recombinant silk-elastinlike protein polymers (SELPs) for TACE. Two SELP compositions, SELP-47K and SELP-815K, with varying lengths of silk and elastin blocks, were investigated to formulate a new embolic that was injectable through commercially available microcatheters. The goal was to develop a composition providing maximal permeation of tumor vasculature while exhibiting effective embolic activity. The SELPs evaluated remain soluble until reaching 37 degrees C, when irreversible transition ensues forming a solid hydrogel network. SELP-815K formulated at 12% w/w with shear processing demonstrated acceptable rheological properties and clear embolic capability under flow conditions in vitro. A rabbit model showed feasibility of embolization in vivo allowing selective occlusion of lobar hepatic arterial branches. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:142 / 152
页数:11
相关论文
共 33 条
[1]   Hepatocellular Carcinoma Incidence, Mortality, and Survival Trends in the United States From 1975 to 2005 [J].
Altekruse, Sean F. ;
McGlynn, Katherine A. ;
Reichman, Marsha E. .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (09) :1485-1491
[2]  
[Anonymous], 2011, SEER CANC STAT REV 1
[3]   Biomimetic Design of Artificial Micro-vasculatures for Tissue Engineering [J].
Barber, Robert W. ;
Emerson, David R. .
ATLA-ALTERNATIVES TO LABORATORY ANIMALS, 2010, 38 :67-79
[4]   Development of Melanoma-Targeted Polymer Micelles by Conjugation of a Melanocortin 1 Receptor (MC1R) Specific Ligand [J].
Barkey, Natalie M. ;
Tafreshi, Narges K. ;
Josan, Jatinder S. ;
De Silva, Channa R. ;
Sill, Kevin N. ;
Hruby, Victor J. ;
Gillies, Robert J. ;
Morse, David L. ;
Vagner, Josef .
JOURNAL OF MEDICINAL CHEMISTRY, 2011, 54 (23) :8078-8084
[5]  
BLUMGART LH, 2007, SURG LIVER BILIARY T, V1
[6]   Quality Improvement Guidelines for Transhepatic Arterial Chemoembolization, Embolization, and Chemotherapeutic Infusion for Hepatic Malignancy [J].
Brown, Daniel B. ;
Nikolic, Boris ;
Covey, Anne M. ;
Nutting, Charles W. ;
Saad, Wael E. A. ;
Salem, Riad ;
Sofocleous, Constantinos T. ;
Sze, Daniel Y. .
JOURNAL OF VASCULAR AND INTERVENTIONAL RADIOLOGY, 2012, 23 (03) :287-294
[7]  
Brown KT, J VASCULAR INTERVENT, V15, P197
[8]   Management of hepatoceullular carcinoma [J].
Bruix, J ;
Sherman, M .
HEPATOLOGY, 2005, 42 (05) :1208-1236
[9]   Management of Hepatocellular Carcinoma: An Update [J].
Bruix, Jordi ;
Sherman, Morris .
HEPATOLOGY, 2011, 53 (03) :1020-1022
[10]   Two Decades of Advances in Hepatocellular Carcinoma Research FOREWORD [J].
Bruix, Jordi ;
Llovet, Josep M. .
SEMINARS IN LIVER DISEASE, 2010, 30 (01) :1-2