Solubility Enhancement of Antidiabetic Drugs Using a Co‐Crystallization Approach

Eustina Batisai

doi:10.1002/open.202100246

Solubility Enhancement of Antidiabetic Drugs Using a Co‐Crystallization Approach

ChemistryOpen ◽

10.1002/open.202100246 ◽

2021 ◽

Vol 10 (12) ◽

pp. 1260-1268

Author(s):

Eustina Batisai

Keyword(s):

Solubility Enhancement ◽

Antidiabetic Drugs

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Abstract #292 Efficacy of Hydroxychloroquine when added in Subjects with Inadequately Controlled Type 2 Diabetes Mellitus Treated with Basal Insulin and Two Other Oral Antidiabetic Drugs

Endocrine Practice ◽

10.1016/s1530-891x(20)46636-4 ◽

2019 ◽

Vol 25 ◽

pp. 119-120

Author(s):

Arjun Baidya ◽

Ajay Chhabra

Keyword(s):

Diabetes Mellitus ◽

Type 2 Diabetes ◽

Type 2 Diabetes Mellitus ◽

Basal Insulin ◽

Antidiabetic Drugs ◽

Oral Antidiabetic Drugs ◽

Oral Antidiabetic

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Treatment of NASH in mice with antidiabetic drugs

10.1055/s-0039-1693546 ◽

2019 ◽

Author(s):

W Jonas ◽

C Gumz ◽

AK Steiner ◽

J Henkel ◽

A Schürmann

Keyword(s):

Antidiabetic Drugs

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Determinant factors for prescription of antidiabetic drugs with beneficial effects on weight

Endocrine Abstracts ◽

10.1530/endoabs.63.p608 ◽

2019 ◽

Author(s):

Manuel Cayon-Blanco ◽

Carolina Garcia-Figueras-Mateos

Keyword(s):

Antidiabetic Drugs ◽

Determinant Factors ◽

Beneficial Effects

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2224-PUB: Comparative Effectiveness of Second-Line Initiation of Basal Insulin Therapy vs. Oral Antidiabetic Drugs Added to Metformin among Patients with Type 2 Diabetes in Taiwan

Diabetes ◽

10.2337/db19-2224-pub ◽

2019 ◽

Vol 68 (Supplement 1) ◽

pp. 2224-PUB

Author(s):

PIN-HAO CHEN ◽

SHIHCHEN KUO ◽

HUANG-TZ OU

Keyword(s):

Type 2 Diabetes ◽

Insulin Therapy ◽

Comparative Effectiveness ◽

Basal Insulin ◽

Antidiabetic Drugs ◽

Second Line ◽

Oral Antidiabetic Drugs ◽

Oral Antidiabetic

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Solubility Enhancement of Weak Bases: Ondansetron

10.26226/morressier.57ea3d69d462b8028d88d494 ◽

2016 ◽

Author(s):

Doaa Alantary

Keyword(s):

Solubility Enhancement ◽

Weak Bases

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Solubility Enhancement Using a Novel, Storage Stable pH Independent EUDRAGIT&[reg] E Formulation

10.26226/morressier.57d6b2bdd462b8028d88d4c6 ◽

2016 ◽

Author(s):

Jitendra Amrutkar

Keyword(s):

Solubility Enhancement

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SOLUBILITY ENHANCEMENT OF VALSARTAN USING MODIFIED POROUS STARCH AS A CARRIER

International Journal of Pharmaceutical Research ◽

10.31838/ijpr/2019.11.01.039 ◽

2019 ◽

Vol 11 (1) ◽

Keyword(s):

Solubility Enhancement

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Effect of PEG 4000 in the crystal engineering of Candesartan Cilexetil for solubility enhancement by Polymer Enriched Bridging Liquid technique

International Journal of Pharmaceutical Research ◽

10.31838/ijpr/2019.11.04.039 ◽

2019 ◽

Vol 11 (4) ◽

Keyword(s):

Crystal Engineering ◽

Candesartan Cilexetil ◽

Solubility Enhancement ◽

Peg 4000

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Solubility Enhancement of Canagliflozin by Binary and Ternary Solid Dispersion Technique

International Journal of Pharmaceutical Research ◽

10.31838/ijpr/2020.12.03.103 ◽

2020 ◽

Vol 12 (03) ◽

Keyword(s):

Solid Dispersion ◽

Solubility Enhancement ◽

Ternary Solid Dispersion ◽

Dispersion Technique

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Faculty Opinions recommendation of Arylsulfonamidothiazoles as a new class of potential antidiabetic drugs. Discovery of potent and selective inhibitors of the 11beta-hydroxysteroid dehydrogenase type 1.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.1008829.113110 ◽

2002 ◽

Author(s):

Thomas W von Geldern

Keyword(s):

Hydroxysteroid Dehydrogenase ◽

Antidiabetic Drugs ◽

Selective Inhibitors ◽

New Class

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