Coated microneedle arrays for transcutaneous delivery of live virus vaccines

Typeset version

 

TY  - JOUR
  - Vrdoljak, A,McGrath, MG,Carey, JB,Draper, SJ,Hill, AVS,O'Mahony, C,Crean, AM,Moore, AC
  - 2012
  - January
  - Journal Of Controlled Release
  - Coated microneedle arrays for transcutaneous delivery of live virus vaccines
  - Validated
  - ()
  - Microneedle Skin Vaccine Poxvirus Adenovirus Spray-coating TRANSDERMAL DELIVERY PATCH SYSTEM ADENOVIRUS TYPE-5 STABILITY CELLS FORMULATIONS IMMUNIZATION TECHNOLOGY PARAMETERS TREHALOSE
  - 159
  - 1
  - 34
  - 42
  - Vaccines are sensitive biologics that require continuous refrigerated storage to maintain their viability. The vast majority of vaccines are also administered using needles and syringes. The need for cold chain storage and the significant logistics surrounding needle-and-syringe vaccination is constraining the success of immunization programs. Recombinant live viral vectors are a promising platform for the development of vaccines against a number of infectious diseases, however these viruses must retain infectivity to be effective. Microneedles offer an effective and painless method for delivery of vaccines directly into skin that in the future could provide solutions to current vaccination issues. Here we investigated methods of coating live recombinant adenovirus and modified vaccinia virus Ankara (MVA) vectors onto solid microneedle arrays. An effective spray-coating method, using conventional pharmaceutical processes, was developed, in tandem with suitable sugar-based formulations, which produces arrays with a unique coating of viable virus in a dry form around the shaft of each microneedle on the array. Administration of live virus-coated microneedle arrays successfully resulted in virus delivery, transcutaneous infection and induced an antibody or CD8(+) T cell response in mice that was comparable to that obtained by needle-and-syringe intradermal immunization. To our knowledge, this is the first report of successful vaccination with recombinant live viral vectored vaccines coated on microneedle delivery devices. (C) 2011 Elsevier B.V. All rights reserved.
  - DOI 10.1016/j.jconrel.2011.12.026
DA  - 2012/01
ER  - 
@article{V146554359,
   = {Vrdoljak,  A and McGrath,  MG and Carey,  JB and Draper,  SJ and Hill,  AVS and O'Mahony,  C and Crean,  AM and Moore,  AC },
   = {2012},
   = {January},
   = {Journal Of Controlled Release},
   = {Coated microneedle arrays for transcutaneous delivery of live virus vaccines},
   = {Validated},
   = {()},
   = {Microneedle Skin Vaccine Poxvirus Adenovirus Spray-coating TRANSDERMAL DELIVERY PATCH SYSTEM ADENOVIRUS TYPE-5 STABILITY CELLS FORMULATIONS IMMUNIZATION TECHNOLOGY PARAMETERS TREHALOSE},
   = {159},
   = {1},
  pages = {34--42},
   = {{Vaccines are sensitive biologics that require continuous refrigerated storage to maintain their viability. The vast majority of vaccines are also administered using needles and syringes. The need for cold chain storage and the significant logistics surrounding needle-and-syringe vaccination is constraining the success of immunization programs. Recombinant live viral vectors are a promising platform for the development of vaccines against a number of infectious diseases, however these viruses must retain infectivity to be effective. Microneedles offer an effective and painless method for delivery of vaccines directly into skin that in the future could provide solutions to current vaccination issues. Here we investigated methods of coating live recombinant adenovirus and modified vaccinia virus Ankara (MVA) vectors onto solid microneedle arrays. An effective spray-coating method, using conventional pharmaceutical processes, was developed, in tandem with suitable sugar-based formulations, which produces arrays with a unique coating of viable virus in a dry form around the shaft of each microneedle on the array. Administration of live virus-coated microneedle arrays successfully resulted in virus delivery, transcutaneous infection and induced an antibody or CD8(+) T cell response in mice that was comparable to that obtained by needle-and-syringe intradermal immunization. To our knowledge, this is the first report of successful vaccination with recombinant live viral vectored vaccines coated on microneedle delivery devices. (C) 2011 Elsevier B.V. All rights reserved.}},
   = {DOI 10.1016/j.jconrel.2011.12.026},
  source = {IRIS}
}
AUTHORSVrdoljak, A,McGrath, MG,Carey, JB,Draper, SJ,Hill, AVS,O'Mahony, C,Crean, AM,Moore, AC
YEAR2012
MONTHJanuary
JOURNAL_CODEJournal Of Controlled Release
TITLECoated microneedle arrays for transcutaneous delivery of live virus vaccines
STATUSValidated
TIMES_CITED()
SEARCH_KEYWORDMicroneedle Skin Vaccine Poxvirus Adenovirus Spray-coating TRANSDERMAL DELIVERY PATCH SYSTEM ADENOVIRUS TYPE-5 STABILITY CELLS FORMULATIONS IMMUNIZATION TECHNOLOGY PARAMETERS TREHALOSE
VOLUME159
ISSUE1
START_PAGE34
END_PAGE42
ABSTRACTVaccines are sensitive biologics that require continuous refrigerated storage to maintain their viability. The vast majority of vaccines are also administered using needles and syringes. The need for cold chain storage and the significant logistics surrounding needle-and-syringe vaccination is constraining the success of immunization programs. Recombinant live viral vectors are a promising platform for the development of vaccines against a number of infectious diseases, however these viruses must retain infectivity to be effective. Microneedles offer an effective and painless method for delivery of vaccines directly into skin that in the future could provide solutions to current vaccination issues. Here we investigated methods of coating live recombinant adenovirus and modified vaccinia virus Ankara (MVA) vectors onto solid microneedle arrays. An effective spray-coating method, using conventional pharmaceutical processes, was developed, in tandem with suitable sugar-based formulations, which produces arrays with a unique coating of viable virus in a dry form around the shaft of each microneedle on the array. Administration of live virus-coated microneedle arrays successfully resulted in virus delivery, transcutaneous infection and induced an antibody or CD8(+) T cell response in mice that was comparable to that obtained by needle-and-syringe intradermal immunization. To our knowledge, this is the first report of successful vaccination with recombinant live viral vectored vaccines coated on microneedle delivery devices. (C) 2011 Elsevier B.V. All rights reserved.
PUBLISHER_LOCATION
ISBN_ISSN
EDITION
URL
DOI_LINKDOI 10.1016/j.jconrel.2011.12.026
FUNDING_BODY
GRANT_DETAILS