Controlled Dissolution Formulations
Controlled Dissolution Formulations is a pharmaceutical formulation strategy that belongs to the class of drug delivery systems in which the rate of drug release is governed by the controlled dissolution of the active agent, distinguished by its reliance on modulating solubility, particle size, matrix composition, or coating properties to achieve a predetermined and sustained release profile over time.
71
Publications
2.9K
Citations
298
Authors
111
Institutions
Publications per year
2017–2026
9
71
Morten Allesø, Norman Chieng, Sönke Rehder et al. · Journal of Controlled Release · 2009 · 270 citations
Anders Sandberg, I. Blomqvist, U. E. Jonsson et al. · European Journal of Clinical Pharmacology · 1988 · 127 citations
Jayanti Nerurkar, H.W. Jun, James C. Price et al. · European Journal of Pharmaceutics and Biopharmaceutics · 2005 · 122 citations
1–5 of 71
298
2
h-index
2
h-index
2
h-index
University of Missouri–Kansas City, United States
2 publications · 125 citations
2
h-index
2
h-index
1–5 of 298
111
Pfizer (United States)
New York, United States
3 h-index
11 publications
417 citations
University of Missouri–Kansas City
Kansas City, United States
3 h-index
7 publications
403 citations

Uniwersytet Komisji Edukacji Narodowej w Krakowie
Krakow, Poland
2 h-index
2 publications
33 citations
Shenyang Pharmaceutical University
Shenyang, China
2 h-index
10 publications
452 citations
Institute of Nuclear Physics, Polish Academy of Sciences
Krakow, Poland
2 h-index
3 publications
55 citations
Bristol-Myers Squibb (United States)
New York, United States
2 h-index
2 publications
125 citations
Jagiellonian University
Krakow, Poland
2 h-index
6 publications
99 citations
University of the Sciences
Philadelphia, United States
2 h-index
4 publications
137 citations
1–8 of 111
16 publications · 591 citations
14
h-index
10 publications · 288 citations
10
h-index
5 publications · 418 citations
5
h-index
4 publications · 141 citations
4
h-index
4 publications · 142 citations
4
h-index
1–5