Atsushi Hamana

Dr. Atsushi Hamana

orcid

Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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16 March 2017 in Molecular Pharmaceutics
Verified
Journal Article
Closed access
AHAtsushi Hamana
Atsushi Hamana
YTYuki Takahashi
Yuki Takahashi
ATAkane Tanioka
Akane Tanioka
MNMakiya Nishikawa
Makiya Nishikawa
Yoshinobu TakakuraYoshinobu Takakura
Yoshinobu Takakura

1 October 2017 in Antiviral Research
Verified
Journal Article
Closed access
AHAtsushi Hamana
Atsushi Hamana
YTYuki Takahashi
Yuki Takahashi
TUTakuro Uchida
Takuro Uchida
MNMakiya Nishikawa
Makiya Nishikawa
MIMichio Imamura
Michio Imamura
Yoshinobu TakakuraYoshinobu Takakura
Yoshinobu Takakura

26 September 2024 in Vaccines
Verified
Journal Article
Open access
PDF file
PKPrashant Kumar
Prashant Kumar
AHAtsushi Hamana
Atsushi Hamana
CBChristopher Bird
Christopher Bird
BDBrandy Dotson
Brandy Dotson
SSSoraia Saleh-Birdjandi
Soraia Saleh-Birdjandi
SJSangeeta Bagai Joshi
Sangeeta Bagai Joshi
In this work, we describe compatibility assessments of a recombinant, trivalent non-replicating rotavirus vaccine (t-NRRV) candidate with a mock trivalent Sabin inactivated polio vaccine (t-sIPV). Both t-sIPV and t-NRRV are incompatible with thimerosal (TH), a preservative commonly used in pediatric pentavalent combination vaccines (DTwP-Hib-HepB) distributed in low- and middle-income countries (LMICs), preventing the development of a heptavalent combination. The compatibility of t-NRRV with a mock DTwP-Hib-HepB formulation is described in a companion paper. This case study highlights the analytical and formulation challenges encountered when combining a mock t-sIPV vaccine (unadjuvanted) with Alhydrogel® (AH) adjuvanted t-NRRV. Selective and stability-indicating competition ELISAs were implemented to monitor antibody binding to each of the six antigens (±AH). Simple mixing caused the undesired desorption of t-NRRV from AH with the concomitant binding of t-sIPV to AH. Although the former effect was mitigated by dialyzing sIPV bulks, decreased sIPV storage stability was observed at accelerated temperatures in the bivalent combination with a rank-ordering of P[8] > P[6] > P[4] and sIPV3 > sIPV2 > sIPV1. The compatibility of AH-adsorbed t-sIPV with alternative preservatives was evaluated, and parabens (methyl, propyl) were identified for potential use in this multi-dose bivalent formulation. Along with a companion paper, the lessons learned are discussed to facilitate the future formulation development of pediatric combination vaccines with new antigens.