Tunable dissolution of poorly soluble gliclazide by surface coating via room-temperature atomic layer deposition

V Viet Phuong Cao (Faculty of Materials Science and Engineering, Phenikaa School of Engineering, Phenikaa University 1 , Hanoi 12116,) T Truong Duc Dinh (Faculty of Materials Science and Engineering, Phenikaa School of Engineering, Phenikaa University 1 , Hanoi 12116,) D Diem-Quyen T. Nguyen (Faculty of Materials Science and Engineering, Phenikaa School of Engineering, Phenikaa University 1 , Hanoi 12116,) M Myung-Jin Jung (School of Materials Science and Engineering, Pusan National University 2 , 30 Jangjeon-Dong Geumjeong-Gu, Busan 46241,) S Se-Hun Kwon (School of Materials Science and Engineering, Pusan National University 2 , 30 Jangjeon-Dong Geumjeong-Gu, Busan 46241,) T Tuan Hiep Tran (Faculty of Pharmacy, Phenikaa School of Medicine and Pharmacy, Phenikaa University 3 , Hanoi 12116,) H Hao Van Bui (Phenikaa Institute for Advanced Study)

Abstract

Gliclazide (GLZ) is a sulfonylurea antidiabetic drug widely used to treat type 2 diabetes mellitus. However, its poor aqueous solubility is a major challenge in drug formulation, often limiting the bioavailability and therapeutic efficacy. In this study, we explore the application of atomic layer deposition (ALD) as a surface engineering technique to enhance the wettability and tailor the dissolution of GLZ. By coating the drug particles with ultra-thin SiO2 films, their wettability is transformed from strongly hydrophobic to highly hydrophilic, promoting a highly dispersed state in an aqueous medium and significantly accelerating the dissolution. More importantly, by controlling the coating thickness, the dissolution rate of GLZ can be tailored, enabling tunable drug dissolution profiles. The results demonstrate the potential of SiO2 ALD not only in overcoming solubility-related limitations but also in providing a method of multipurpose design for controlled drug delivery. Given its compatibility with pharmaceutical manufacturing, our approach presents a promising pathway to enhance bioavailability and optimize the release kinetics of other poorly soluble drugs.

Article Details

Volume / Issue Vol. 164, Issue 22
Published June 14, 2026
ISSN 0021-9606
Publisher American Institute of Physics

Journal Info

The Journal of Chemical Physics

American Institute of Physics

ISSN: 0021-9606 Physical Sciences

Authors (7)

V

Viet Phuong Cao

Faculty of Materials Science and Engineering, Phenikaa School of Engineering, Phenikaa University 1 , Hanoi 12116,

T

Truong Duc Dinh

Faculty of Materials Science and Engineering, Phenikaa School of Engineering, Phenikaa University 1 , Hanoi 12116,

D

Diem-Quyen T. Nguyen

Faculty of Materials Science and Engineering, Phenikaa School of Engineering, Phenikaa University 1 , Hanoi 12116,

M

Myung-Jin Jung

School of Materials Science and Engineering, Pusan National University 2 , 30 Jangjeon-Dong Geumjeong-Gu, Busan 46241,

S

Se-Hun Kwon

School of Materials Science and Engineering, Pusan National University 2 , 30 Jangjeon-Dong Geumjeong-Gu, Busan 46241,

T

Tuan Hiep Tran

Faculty of Pharmacy, Phenikaa School of Medicine and Pharmacy, Phenikaa University 3 , Hanoi 12116,

H

Hao Van Bui

Phenikaa Institute for Advanced Study