TY - JOUR
T1 - Transdermal Transmission Blocking Vaccine for Malaria using a Solid-in-Oil Dispersion
AU - Tanaka, Keisuke
AU - Minamihata, Kosuke
AU - Wakabayashi, Rie
AU - Lee, Jae Man
AU - Miyata, Takeshi
AU - Kusakabe, Takahiro
AU - Kamiya, Noriho
AU - Goto, Masahiro
N1 - Funding Information:
The authors thank Professor Y. Katayama and Associate professor T. Mori for their support in carrying out the animal experiments. The authors acknowledge financial support ( JSPS KAKENHI grant numbers JP16H06369 and JP19J21032 ) from the Ministry of Education, Culture, Sports, Science, and Technology of Japan. We thank Victoria Muir, PhD, from Edanz ( https://jp.edanz.com/ac ) for editing a draft of this manuscript.
Publisher Copyright:
© 2022 American Pharmacists Association
PY - 2022
Y1 - 2022
N2 - Malaria is a mosquito-borne infectious disease that is widespread in developing countries. Malaria vaccines are important in efforts to eradicate malaria; however, vaccines are usually administered by injection, which requires medical personnel and has a risk of causing infection. Transdermal vaccines can be administered without damaging the skin and thus are ideal for the prevention of malaria. However, the stratum corneum forms a "brick and mortar" like structure in which stratum corneum cells are embedded in a hydrophobic matrix composed of lipids, which strongly inhibits the permeation of hydrophilic substances. In the present study, we designed a transdermal vaccine against vivax malaria using a solid-in-oil (S/O) dispersion. The S/O dispersion of a transmission blocking vaccine candidate, Pvs25 from Plasmodium vivax, showed higher skin penetration than that of the aqueous solution. Mice immunized with the S/O dispersion generated antibodies at similar titers as the mice immunized by injection, over the mid- to long-term. These results provide information for the development of transdermally administered malaria vaccines toward the eradication of malaria.
AB - Malaria is a mosquito-borne infectious disease that is widespread in developing countries. Malaria vaccines are important in efforts to eradicate malaria; however, vaccines are usually administered by injection, which requires medical personnel and has a risk of causing infection. Transdermal vaccines can be administered without damaging the skin and thus are ideal for the prevention of malaria. However, the stratum corneum forms a "brick and mortar" like structure in which stratum corneum cells are embedded in a hydrophobic matrix composed of lipids, which strongly inhibits the permeation of hydrophilic substances. In the present study, we designed a transdermal vaccine against vivax malaria using a solid-in-oil (S/O) dispersion. The S/O dispersion of a transmission blocking vaccine candidate, Pvs25 from Plasmodium vivax, showed higher skin penetration than that of the aqueous solution. Mice immunized with the S/O dispersion generated antibodies at similar titers as the mice immunized by injection, over the mid- to long-term. These results provide information for the development of transdermally administered malaria vaccines toward the eradication of malaria.
UR - http://www.scopus.com/inward/record.url?scp=85142295452&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85142295452&partnerID=8YFLogxK
U2 - 10.1016/j.xphs.2022.10.031
DO - 10.1016/j.xphs.2022.10.031
M3 - Article
C2 - 36334812
AN - SCOPUS:85142295452
SN - 0022-3549
JO - Journal of Pharmaceutical Sciences
JF - Journal of Pharmaceutical Sciences
ER -