TY - JOUR
T1 - Dry-coated microprojection array patches for targeted delivery of immunotherapeutics to the skin
AU - Chen, Xianfeng
AU - Prow, Tarl W.
AU - Crichton, Michael L.
AU - Jenkins, Derek W K
AU - Roberts, Michael S.
AU - Frazer, Ian H.
AU - Fernando, Germain J P
AU - Kendall, Mark A F
PY - 2009/11/3
Y1 - 2009/11/3
N2 - Dry-coated microprojections (MPs) deliver vaccine to abundant immunogenic cells within the skin to induce immune responses. Success in this targeted vaccine delivery relies on overcoming the challenges of dry-coating the vaccine onto the very small (≤ 90 μm length) and densely packed (~ 20,000 cm- 2) MPs. In this paper, we show that a gas-jet drying coating method achieves the desired uniform coating. The coating approach is robustly demonstrated on compounds representative of a range of immunotherapeutics (e.g. DNA, proteins), with each uniformly coated on thousands of MPs. Furthermore, the dry-coating remains intact during skin insertion, and then releases within the wet skin cellular environment within 3 min. Finally, we applied ovalbumin protein coated MP patches to immunise mice, achieving comparable antibody levels (p = 0.08) with needle and syringe intramuscular injection. In summary, this paper presents a simple, practical and versatile method to achieve uniform coating on very small and densely packed MPs for a needle-free and targeted vaccine delivery technology.
AB - Dry-coated microprojections (MPs) deliver vaccine to abundant immunogenic cells within the skin to induce immune responses. Success in this targeted vaccine delivery relies on overcoming the challenges of dry-coating the vaccine onto the very small (≤ 90 μm length) and densely packed (~ 20,000 cm- 2) MPs. In this paper, we show that a gas-jet drying coating method achieves the desired uniform coating. The coating approach is robustly demonstrated on compounds representative of a range of immunotherapeutics (e.g. DNA, proteins), with each uniformly coated on thousands of MPs. Furthermore, the dry-coating remains intact during skin insertion, and then releases within the wet skin cellular environment within 3 min. Finally, we applied ovalbumin protein coated MP patches to immunise mice, achieving comparable antibody levels (p = 0.08) with needle and syringe intramuscular injection. In summary, this paper presents a simple, practical and versatile method to achieve uniform coating on very small and densely packed MPs for a needle-free and targeted vaccine delivery technology.
KW - Gas-jet drying coating
KW - Microprojections
KW - Targeted vaccine delivery
UR - http://www.scopus.com/inward/record.url?scp=70349322619&partnerID=8YFLogxK
U2 - 10.1016/j.jconrel.2009.06.029
DO - 10.1016/j.jconrel.2009.06.029
M3 - Article
C2 - 19577597
AN - SCOPUS:70349322619
SN - 0168-3659
VL - 139
SP - 212
EP - 220
JO - Journal of Controlled Release
JF - Journal of Controlled Release
IS - 3
ER -