Noriho Kamiya

Dr. Noriho Kamiya

orcid

Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

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

Representative Publications

View All Publications
15 May 2018 in Molecular Pharmaceutics
Verified
Journal Article
Closed access
MCMD. Raihan Chowdhury
MD. Raihan Chowdhury
Rahman Md MoshikurRahman Md Moshikur
Rahman Md Moshikur
RWRie Wakabayashi
Rie Wakabayashi
YTYoshiro Tahara
Yoshiro Tahara
NKNoriho Kamiya
Noriho Kamiya
Masahiro GotoMasahiro Goto
Masahiro Goto

4 March 2020 in ACS Sustainable Chemistry & Engineering
Verified
Journal Article
Closed access
KAKorban Ali
Korban Ali
Rahman Md MoshikurRahman Md Moshikur
Rahman Md Moshikur
RWRie Wakabayashi
Rie Wakabayashi
MMMuhammad Muniruzzaman
Muhammad Muniruzzaman
NKNoriho Kamiya
Noriho Kamiya
Masahiro GotoMasahiro Goto
Masahiro Goto

1 May 2015 in Enzyme and Microbial Technology
Verified
Journal Article
Closed access
GGGeisa A.L. Gonçalves
Geisa A.L. Gonçalves
YTYusaku Takasugi
Yusaku Takasugi
LJLili Jia
Lili Jia
YMYutaro Mori
Yutaro Mori
SNShuhei Noda
Shuhei Noda
NKNoriho Kamiya
Noriho Kamiya

24 January 2025 in Marine Drugs
Verified
Journal Article
Open access
PDF file
RPRizfi Fariz Pari
Rizfi Fariz Pari
UUUju Uju
Uju Uju
SHSafrina Dyah Hardiningtyas
Safrina Dyah Hardiningtyas
Wahyu RamadhanWahyu Ramadhan
Wahyu Ramadhan
RWRie Wakabayashi
Rie Wakabayashi
NKNoriho Kamiya
Noriho Kamiya
Green seaweed is currently underused compared with other major seaweed types. Many scientists have reported applications of the green seaweed Ulva in various fields in recent years, which makes it a candidate for biomass production in industrial biorefineries. Ulva contains a unique polysaccharide called ulvan, which is being considered for medicinal and pharmacological applications. Ulvan is a sulfated polysaccharide including rhamnose and glucuronic acid residues, which has a range of bioactivities, including immunomodulatory, antimicrobial, and anticoagulant properties. The biocompatibility of ulvan makes it a versatile candidate for biomaterial design. This review presents an in-depth analysis of the potential applications of ulvan, starting with extraction methods and structural/biological characterization and moving on to biomaterial design. We also highlight the advantages of ulvan over traditional seaweed polysaccharides such as agar, carrageenan, and alginate.

1 May 2020 in International Journal of Pharmaceutics
Verified
Journal Article
Closed access
MIMd. Rafiqul Islam
Md. Rafiqul Islam
RCRaihan Chowdhury
Raihan Chowdhury
RWRie Wakabayashi
Rie Wakabayashi
YTYoshiro Tahara
Yoshiro Tahara
NKNoriho Kamiya
Noriho Kamiya
Masahiro GotoMasahiro Goto
Masahiro Goto

24 April 2020 in Pharmaceutics
Verified
Journal Article
Open access
PDF file
MIMd. Rafiqul Islam
Md. Rafiqul Islam
MCMD. Raihan Chowdhury
MD. Raihan Chowdhury
RWRie Wakabayashi
Rie Wakabayashi
NKNoriho Kamiya
Noriho Kamiya
MMMuhammad Muniruzzaman
Muhammad Muniruzzaman
Masahiro GotoMasahiro Goto
Masahiro Goto
The transdermal delivery of sparingly soluble drugs is challenging due to of the need for a drug carrier. In the past few decades, ionic liquid (IL)-in-oil microemulsions (IL/O MEs) have been developed as potential carriers. By focusing on biocompatibility, we report on an IL/O ME that is designed to enhance the solubility and transdermal delivery of the sparingly soluble drug, acyclovir. The prepared MEs were composed of a hydrophilic IL (choline formate, choline lactate, or choline propionate) as the non-aqueous polar phase and a surface-active IL (choline oleate) as the surfactant in combination with sorbitan laurate in a continuous oil phase. The selected ILs were all biologically active ions. Optimized pseudo ternary phase diagrams indicated the MEs formed thermodynamically stable, spherically shaped, and nano-sized (90%) with the ME compared with Dulbecco’s phosphate-buffered saline, indicates the biocompatibility of the ME. Therefore, we conclude that IL/O ME may be a promising nano-carrier for the transdermal delivery of sparingly soluble drugs.