Silk Reservoirs for Local Delivery of Cisplatin for Neuroblastoma Treatment: In Vitro and In Vivo Evaluations

被引:16
作者
Yavuz, Burcin [1 ]
Zeki, Jasmine [2 ]
Taylor, Jordan [2 ]
Harrington, Kristin [1 ]
Coburn, Jeannine M. [1 ,3 ]
Ikegaki, Naohiko [4 ]
Kaplan, David L. [1 ]
Chiu, Bill [2 ]
机构
[1] Tufts Univ, Dept Biomed Engn, Medford, MA 02155 USA
[2] Stanford Univ, Dept Surg, Stanford, CA 94305 USA
[3] Worcester Polytech Inst, Dept Biomed Engn, Worcester, MA 01609 USA
[4] Univ Illinois, Dept Anat & Cell Biol, Chicago, IL 60612 USA
基金
美国国家卫生研究院;
关键词
cancer chemotherapy; drug delivery system; biomaterials; controlled release; solid dosage forms; site-specific delivery; DRUG-RELEASE; FILMS; CHEMOTHERAPY; PHARMACOKINETICS; NANOPARTICLES; VINCRISTINE; HYDROGELS; KINETICS; SYSTEM; RODS;
D O I
10.1016/j.xphs.2019.03.019
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Neuroblastoma is the most common extracranial childhood tumor, and current treatment requires surgical resection and multidrug chemotherapy. Local, perioperative delivery of chemotherapeutics is a promising treatment method for solid tumors that require surgical removal. In this study, we have aimed to develop a controlled-release implant system to deliver cisplatin in tumor or tumor resection area. Silk fibroin, a biodegradable, nonimmunogenic biopolymer was used to encapsulate different doses of cisplatin in a reservoir system. The physical integrity of the reservoirs was characterized by evaluating the crystalline structure of silk secondary structure using FTIR spectroscopy. The in vitro release of cisplatin was evaluated in phosphate-buffered saline at 37 degrees C, and the reservoirs were able to release the drug up to 30 days. The cytotoxicity of cisplatin and cisplatin reservoirs were tested on KELLY cells. Cytotoxicity data showed 3.2 mu g/mL cisplatin was required to kill 50% of the cell population, and the released cisplatin from the silk reservoirs showed significant cytotoxicity up to 21 days. Intratumoral implantation of silk reservoirs into an orthotopic neuroblastoma mouse model decreased tumor growth significantly when compared with control subjects. These results suggest that silk reservoirs are promising carriers for cisplatin delivery to the tumor site. (c) 2019 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:2748 / 2755
页数:8
相关论文
共 45 条
[11]  
Dash S, 2010, ACTA POL PHARM, V67, P217
[12]   INTRATUMOURAL ADMINISTRATION OF CISPLATIN IN SLOW-RELEASE DEVICES .2. PHARMACOKINETICS AND INTRATUMOURAL DISTRIBUTION [J].
DEURLOO, MJM ;
KOP, W ;
VANTELLINGEN, O ;
BARTELINK, H ;
BEGG, AC .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1991, 27 (05) :347-353
[13]   Nanoparticle formulations of cisplatin for cancer therapy [J].
Duan, Xiaopin ;
He, Chunbai ;
Kron, Stephen J. ;
Lin, Wenbin .
WILEY INTERDISCIPLINARY REVIEWS-NANOMEDICINE AND NANOBIOTECHNOLOGY, 2016, 8 (05) :776-791
[14]   Drug release kinetics and transport mechanisms of non-degradable and degradable polymeric delivery systems [J].
Fu, Yao ;
Kao, Weiyuan John .
EXPERT OPINION ON DRUG DELIVERY, 2010, 7 (04) :429-444
[15]  
HAGIWARA A, 1993, ANTI-CANCER DRUG DES, V8, P463
[16]   Clinical Considerations of Focal Drug Delivery in Cancer Treatment [J].
Harris, Jamie ;
Klonoski, Samuel C. ;
Chiu, Bill .
CURRENT DRUG DELIVERY, 2017, 14 (05) :588-596
[17]  
Holland C, 2019, ADV HLTH CARE MAT, V8, P1
[18]   Determining beta-sheet crystallinity in fibrous proteins by thermal analysis and infrared spectroscopy [J].
Hu, Xiao ;
Kaplan, David ;
Cebe, Peggy .
MACROMOLECULES, 2006, 39 (18) :6161-6170
[19]   The development of SERI® Surgical Scaffold, an engineered biological scaffold [J].
Jewell, Mark ;
Daunch, William ;
Bengtson, Bradley ;
Mortarino, Enrico .
PHARMACEUTICAL SCIENCE TO IMPROVE THE HUMAN CONDITION: PRIX GALIEN 2014, 2015, 1358 :44-55
[20]  
Khanna C, 2002, IN VIVO, V16, P77