Thermostabilization of inactivated polio vaccine in PLGA-based microspheres for pulsatile release

被引:45
|
作者
Tzeng, Stephany Y. [1 ]
Guarecuco, Rohiverth [1 ]
McHugh, Kevin J. [1 ]
Rose, Sviatlana [1 ]
Rosenberg, Evan M. [1 ]
Zeng, Yingying [1 ]
Langer, Robert [1 ]
Jaklenec, Ana [1 ]
机构
[1] MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
关键词
Drug delivery; Vaccine delivery; Single-administration vaccines; Controlled release kinetics; Vaccine stability; BIODEGRADABLE MICROSPHERES; POLYMER MICROSPHERES; THERMAL-STABILITY; DRUG-DELIVERY; PROTEIN; MICROENCAPSULATION; STABILIZATION; IMMUNIZATION; MECHANISMS; CHALLENGES;
D O I
10.1016/j.jconrel.2016.05.012
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Vaccines are a critical clinical tool in preventing illness and death due to infectious diseases and are regularly administered to children and adults across the globe. In order to obtain full protection from many vaccines, an individual needs to receive multiple doses over the course of months. However, vaccine administration in developing countries is limited by the difficulty in consistently delivering a second or third dose, and some vaccines, including the inactivated polio vaccine (IPV), must be injected more than once for efficacy. In addition, IPV does not remain stable over time at elevated temperatures, such as those it would encounter over time in the body if it were to be injected as a single-administration vaccine. In this manuscript, we describe microspheres composed of poly(lactic-co-glycolic acid) (PLGA) that can encapsulate IPV along with stabilizing excipients and release immunogenic IPV over the course of several weeks. Additionally, pH-sensitive, cationic dopants such as Eudragit E polymer caused clinically relevant amounts of stable IPV release upon degradation of the PLGA matrix. Specifically, IPV was released in two separate bursts, mimicking the delivery of two boluses approximately one month apart. In one of our top formulations, 1.4, 1.1, and 1.2 doses of the IPV serotype 1, 2, and 3, respectively, were released within the first few days from 50 mg of particles. During the delayed, second burst, 0.5, 0.8, and 0.6 doses of each serotype, respectively, were released; thus, 50 mg of these particles released approximately two clinical doses spaced a month apart. Immunization of rats with the leading microsphere formulation showed more robust and long-lasting humoral immune response compared to a single bolus injection and was statistically non-inferior from two bolus injections spaced 1 month apart. By minimizing the number of administrations of a vaccine, such as IPV, this technology can serve as a tool to aid in the eradication of polio and other infectious diseases for the improvement of global health. (C) 2016 The Authors. Published by Elsevier B.V.
引用
收藏
页码:101 / 113
页数:13
相关论文
共 50 条
  • [1] Controlled-release of fluazinam from biodegradable PLGA-based microspheres
    Wang, Qi
    Shen, Mengfei
    Li, Wenjing
    Li, Wanwan
    Zhang, Fang
    JOURNAL OF ENVIRONMENTAL SCIENCE AND HEALTH PART B-PESTICIDES FOOD CONTAMINANTS AND AGRICULTURAL WASTES, 2019, 54 (10) : 810 - 816
  • [2] Development of near zero-order release PLGA-based microspheres of a novel antipsychotic
    Zhao, Jinlong
    Wang, Lexi
    Fan, Chunyu
    Yu, Kongtong
    Liu, Ximing
    Zhao, Xiaolei
    Wang, Dan
    Liu, Wenhua
    Su, Zhengxing
    Sun, Fengying
    Li, Youxin
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2017, 516 (1-2) : 32 - 38
  • [3] PLGA-BASED TOLTERODINE MICROSPHERES: OWN HIGH DRUG-LOADING AND LONG RELEASE PERIOD
    Liu, Na
    Liu, Ximing
    Meng, Fanxin
    Liu, Jiaxin
    Lee, Robert J.
    Li, Youxin
    Teng, Lirong
    Sun, Fengying
    INDIAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2018, 80 (01) : 7 - 7
  • [4] Optimising the controlled release of dexamethasone from a new generation of PLGA-based microspheres intended for intravitreal administration
    Rodriguez Villanueva, Javier
    Bravo-Osuna, Irene
    Herrero-Vanrell, Rocio
    Molina Martinez, Irene Teresa
    Guzman Navarro, Manuel
    EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2016, 92 : 287 - 297
  • [5] Precise Drug Delivery by Using PLGA-Based Microspheres and Optical Manipulators
    Liu, Hongbo
    Li, Xiaojian
    Wei, Tanyong
    Xu, Shisan
    Chen, Shuxun
    Cheng, Shuk Han
    Sun, Dong
    IEEE TRANSACTIONS ON NANOBIOSCIENCE, 2020, 19 (02) : 192 - 202
  • [6] PLGA-Based Microparticles for the Sustained Release of BMP-2
    Kirby, Giles T. S.
    White, Lisa J.
    Rahman, Cheryl V.
    Cox, Helen C.
    Qutachi, Omar
    Rose, Felicity R. A. J.
    Hutmacher, Dietmar W.
    Shakesheff, Kevin M.
    Woodruff, Maria A.
    POLYMERS, 2011, 3 (01) : 571 - 586
  • [7] Extended pulsated drug release from PLGA-based minirods
    Danyuo, Y.
    Oberaifo, O. E.
    Obayemi, J. D.
    Dozie-Nwachukwu, S.
    Ani, C. J.
    Odusanya, O. S.
    Kana, M. G. Zebaze
    Malatesta, K.
    Soboyejo, W. O.
    JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2017, 28 (04)
  • [8] Controlled release of oligonucleotide/polyethyleneimine complexes from PLGA-based microspheres: potential of spray-drying technique
    Ungaro, F
    De Rosa, G
    Quaglia, F
    Fattal, E
    La Rotonda, MI
    JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, 2005, 15 (02) : 137 - 143
  • [9] Extended pulsated drug release from PLGA-based minirods
    Y. Danyuo
    O. E. Oberaifo
    J. D. Obayemi
    S. Dozie-Nwachukwu
    C. J. Ani
    O. S. Odusanya
    M. G. Zebaze Kana
    K. Malatesta
    W. O. Soboyejo
    Journal of Materials Science: Materials in Medicine, 2017, 28
  • [10] Development of PLGA-based itraconazole injectable nanospheres for sustained release
    Bian, Xiaomei
    Liang, Su
    John, Jyothy
    Hsiao, Cheng-Hui
    Wei, Xin
    Liang, Dong
    Xie, Huan
    INTERNATIONAL JOURNAL OF NANOMEDICINE, 2013, 8 : 4521 - 4531