Single shot tetanus vaccine manufactured by a supercritical fluid encapsulation technology

被引:22
作者
Baxendale, Aj [1 ]
van Hooff, P. [1 ]
Durrant, L. G. [2 ]
Spendlove, I. [2 ]
Howdle, S. M. [1 ,3 ]
Woods, H. M. [1 ]
Whitaker, M. J. [1 ]
Davies, O. R. [1 ]
Naylor, A. [1 ]
Lewis, A. L. [1 ]
Illum, L. [1 ]
机构
[1] Crit Pharmaceut Ltd, BioCity Nottingham, Nottingham NG1 1GF, England
[2] Univ Nottingham, City Hosp, Acad Dept Clin Oncol, Nottingham NG5 1PB, England
[3] Univ Nottingham, Sch Chem, Nottingham NG7 2RD, England
基金
英国生物技术与生命科学研究理事会;
关键词
Tetanus toxoid; Microparticles; PLA; Single shot vaccine; Vaccine delivery system; POLY(LACTIC-CO-GLYCOLIC ACID) MICROPARTICLES; BIODEGRADABLE POLYMER PARTICLES; PLGA MICROSPHERES; DELIVERY-SYSTEMS; IMMUNOLOGICAL EVALUATION; IMMUNE-RESPONSE; ADJUVANTS; RELEASE; IMMUNOGENICITY; IMMUNIZATION;
D O I
10.1016/j.ijpharm.2011.04.053
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Single shot vaccines of tetanus toxoid (TT) were manufactured using the NanoMix (TM) process - a low temperature solvent free encapsulation technology using supercritical fluids. The formulations were injected into mice, and compared to multiple injections of a commercially available alum adsorbed TT vaccine. After 5 months the antibody titres were found to be similar for both the alum adsorbed and microparticle formulations, demonstrating for the first time the potential of formulating antigens in PLA microparticles using the supercritical fluid (NanoMix (TM)) technique to produce single shot vaccines. The results are likely to be due to the maintenance of toxoid bioactivity and some degree of sustained release of the encapsulated antigens, resulting in repeated stimulation of antigen presenting cells eliminating the need for multiple immunisations. This demonstrates the potential of this supercritical fluid processing technique to reduce the need for booster doses in a vaccine regimen. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:147 / 154
页数:8
相关论文
共 33 条
[1]
Chitosan microparticles as oral delivery system for tetanus toxoid [J].
Ahire, Vijay J. ;
Sawant, Krutika K. ;
Doshi, Jignesh B. ;
Ravetkar, Satish D. .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2007, 33 (10) :1112-1124
[2]
Parameters influencing the antigen release from spray-dried poly(DL-lactide) microparticles [J].
Baras, B ;
Benoit, MA ;
Gillard, J .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2000, 200 (01) :133-145
[3]
Systemic and Mucosal Delivery of Drugs within Polymeric Microparticles Produced by Spray Drying [J].
Bowey, Kristen ;
Neufeld, Ronald J. .
BIODRUGS, 2010, 24 (06) :359-377
[4]
Applications of supercritical CO2 in the fabrication of polymer systems for drug delivery and tissue engineering [J].
Davies, Owen R. ;
Lewis, Andrew L. ;
Whitaker, Martin J. ;
Tai, Hongyun ;
Shakesheff, Kevin M. ;
Howdle, Steven M. .
ADVANCED DRUG DELIVERY REVIEWS, 2008, 60 (03) :373-387
[5]
Nasal vaccines [J].
Davis, SS .
ADVANCED DRUG DELIVERY REVIEWS, 2001, 51 (1-3) :21-42
[6]
BIODEGRADABLE AND BIOCOMPATIBLE POLY(DL-LACTIDE-CO-GLYCOLIDE) MICROSPHERES AS AN ADJUVANT FOR STAPHYLOCOCCAL ENTEROTOXIN-B TOXOID WHICH ENHANCES THE LEVEL OF TOXIN-NEUTRALIZING ANTIBODIES [J].
ELDRIDGE, JH ;
STAAS, JK ;
MEULBROEK, JA ;
TICE, TR ;
GILLEY, RM .
INFECTION AND IMMUNITY, 1991, 59 (09) :2978-2986
[7]
Pharmaceutical and immunological evaluation of a single-dose hepatitis B vaccine using PLGA microspheres [J].
Feng, L ;
Qi, XR ;
Zhou, XJ ;
Maitani, Y ;
Wang, SC ;
Jiang, Y ;
Nagai, T .
JOURNAL OF CONTROLLED RELEASE, 2006, 112 (01) :35-42
[8]
Supercritical fluid mixing: preparation of thermally sensitive polymer composites containing bioactive materials [J].
Howdle, SM ;
Watson, MS ;
Whitaker, MJ ;
Popov, VK ;
Davies, MC ;
Mandel, FS ;
Wang, JD ;
Shakesheff, KM .
CHEMICAL COMMUNICATIONS, 2001, (01) :109-110
[9]
Polymeric lamellar substrate particles for intranasal vaccination [J].
Jabbal-Gill, I ;
Lin, W ;
Kistner, O ;
Davis, SS ;
Illum, L .
ADVANCED DRUG DELIVERY REVIEWS, 2001, 51 (1-3) :97-111
[10]
Development of a single dose tetanus toxoid formulation based on polymeric microspheres: a comparative study of poly(D,L-lactic-co-glycolic acid) versus chitosan microspheres [J].
Jaganathan, KS ;
Rao, YUB ;
Singh, P ;
Prabakaran, D ;
Gupta, S ;
Jain, A ;
Vyas, SP .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2005, 294 (1-2) :23-32