Production of dissolvable microneedles using an atomised spray process: Effect of microneedle composition on skin penetration.

Typeset version

 

TY  - JOUR
  - McGrath MG, Vucen S, Vrdoljak A, Kelly A, O'Mahony C, Crean AM, Moore AC.
  - 2013
  - May
  - European Journal of Pharmaceutical Science
  - Production of dissolvable microneedles using an atomised spray process: Effect of microneedle composition on skin penetration.
  - In Press
  - ()
  - Epub ahead of print
  - Dissolvable microneedles offer an attractive delivery system for transdermal drug and vaccine delivery. They are most commonly formed by filling a microneedle mold with liquid formulation using vacuum or centrifugation to overcome the constraints of surface tension and solution viscosity. Here, we demonstrate a novel microneedle fabrication method employing an atomised spray technique that minimises the effects of the liquid surface tension and viscosity when filling molds. This spray method was successfully used to fabricate dissolvable microneedles (DMN) from a wide range of sugars (trehalose, fructose and raffinose) and polymeric materials (polyvinyl alcohol, polyvinylpyrrolidone, carboxymethylcellulose, hydroxypropylmethylcellulose and sodium alginate). Fabrication by spraying produced microneedles with amorphous content using single sugar compositions. These microneedles displayed sharp tips and had complete fidelity to the master silicon template. Using a method to quantify the consistency of DMN penetration into different skin layers, we demonstrate that the material of construction significantly influenced the extent of skin penetration. We demonstrate that this spraying method can be adapted to produce novel laminate-layered as well as horizontally-layered DMN arrays. To our knowledge, this is the first report documenting the use of an atomising spray, at ambient, mild processing conditions, to create dissolvable microneedle arrays that can possess novel, laminate layering.
  - http://0-www.sciencedirect.com.library.ucc.ie/science/article/pii/S0939641113001896
  - 10.1016/j.ejpb.2013.04.023. [Epub ahead of print]
DA  - 2013/05
ER  - 
@article{V215228144,
   = {McGrath MG,  Vucen S and  Vrdoljak A,  Kelly A and  O'Mahony C,  Crean AM and  Moore AC. },
   = {2013},
   = {May},
   = {European Journal of Pharmaceutical Science},
   = {Production of dissolvable microneedles using an atomised spray process: Effect of microneedle composition on skin penetration.},
   = {In Press},
   = {()},
   = {Epub ahead of print},
   = {{Dissolvable microneedles offer an attractive delivery system for transdermal drug and vaccine delivery. They are most commonly formed by filling a microneedle mold with liquid formulation using vacuum or centrifugation to overcome the constraints of surface tension and solution viscosity. Here, we demonstrate a novel microneedle fabrication method employing an atomised spray technique that minimises the effects of the liquid surface tension and viscosity when filling molds. This spray method was successfully used to fabricate dissolvable microneedles (DMN) from a wide range of sugars (trehalose, fructose and raffinose) and polymeric materials (polyvinyl alcohol, polyvinylpyrrolidone, carboxymethylcellulose, hydroxypropylmethylcellulose and sodium alginate). Fabrication by spraying produced microneedles with amorphous content using single sugar compositions. These microneedles displayed sharp tips and had complete fidelity to the master silicon template. Using a method to quantify the consistency of DMN penetration into different skin layers, we demonstrate that the material of construction significantly influenced the extent of skin penetration. We demonstrate that this spraying method can be adapted to produce novel laminate-layered as well as horizontally-layered DMN arrays. To our knowledge, this is the first report documenting the use of an atomising spray, at ambient, mild processing conditions, to create dissolvable microneedle arrays that can possess novel, laminate layering.}},
   = {http://0-www.sciencedirect.com.library.ucc.ie/science/article/pii/S0939641113001896},
   = {10.1016/j.ejpb.2013.04.023. [Epub ahead of print]},
  source = {IRIS}
}
AUTHORSMcGrath MG, Vucen S, Vrdoljak A, Kelly A, O'Mahony C, Crean AM, Moore AC.
YEAR2013
MONTHMay
JOURNAL_CODEEuropean Journal of Pharmaceutical Science
TITLEProduction of dissolvable microneedles using an atomised spray process: Effect of microneedle composition on skin penetration.
STATUSIn Press
TIMES_CITED()
SEARCH_KEYWORD
VOLUMEEpub ahead of print
ISSUE
START_PAGE
END_PAGE
ABSTRACTDissolvable microneedles offer an attractive delivery system for transdermal drug and vaccine delivery. They are most commonly formed by filling a microneedle mold with liquid formulation using vacuum or centrifugation to overcome the constraints of surface tension and solution viscosity. Here, we demonstrate a novel microneedle fabrication method employing an atomised spray technique that minimises the effects of the liquid surface tension and viscosity when filling molds. This spray method was successfully used to fabricate dissolvable microneedles (DMN) from a wide range of sugars (trehalose, fructose and raffinose) and polymeric materials (polyvinyl alcohol, polyvinylpyrrolidone, carboxymethylcellulose, hydroxypropylmethylcellulose and sodium alginate). Fabrication by spraying produced microneedles with amorphous content using single sugar compositions. These microneedles displayed sharp tips and had complete fidelity to the master silicon template. Using a method to quantify the consistency of DMN penetration into different skin layers, we demonstrate that the material of construction significantly influenced the extent of skin penetration. We demonstrate that this spraying method can be adapted to produce novel laminate-layered as well as horizontally-layered DMN arrays. To our knowledge, this is the first report documenting the use of an atomising spray, at ambient, mild processing conditions, to create dissolvable microneedle arrays that can possess novel, laminate layering.
PUBLISHER_LOCATION
ISBN_ISSN
EDITION
URLhttp://0-www.sciencedirect.com.library.ucc.ie/science/article/pii/S0939641113001896
DOI_LINK10.1016/j.ejpb.2013.04.023. [Epub ahead of print]
FUNDING_BODY
GRANT_DETAILS