Arvind Singh Chandel

Dr. Arvind Singh Chandel

Faculty of Medicine The Univesrisity of Tokyo Japan
orcid
Marie Curie Postdoctoral Researcher

Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

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

Representative Publications

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23 August 2022 in Biomedicines
Verified
Journal Article
Open access
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DBDixit V Bhalani
Dixit V Bhalani
NBNutan Bhingaradiya
Nutan Bhingaradiya
AKAvinash Kumar
Avinash Kumar
Arvind Singh ChandelArvind Singh Chandel
Arvind Singh Chandel
The low water solubility of pharmacoactive molecules limits their pharmacological potential, but the solubility parameter cannot compromise, and so different approaches are employed to enhance their bioavailability. Pharmaceutically active molecules with low solubility convey a higher risk of failure for drug innovation and development. Pharmacokinetics, pharmacodynamics, and several other parameters, such as drug distribution, protein binding and absorption, are majorly affected by their solubility. Among all pharmaceutical dosage forms, oral dosage forms cover more than 50%, and the drug molecule should be water-soluble. For good therapeutic activity by the drug molecule on the target site, solubility and bioavailability are crucial factors. The pharmaceutical industry’s screening programs identified that around 40% of new chemical entities (NCEs) face various difficulties at the formulation and development stages. These pharmaceuticals demonstrate less solubility and bioavailability. Enhancement of the bioavailability and solubility of drugs is a significant challenge in the area of pharmaceutical formulations. According to the Classification of Biopharmaceutics, Class II and IV drugs (APIs) exhibit poor solubility, lower bioavailability, and less dissolution. Various technologies are discussed in this article to improve the solubility of poorly water-soluble drugs, for example, the complexation of active molecules, the utilization of emulsion formation, micelles, microemulsions, cosolvents, polymeric micelle preparation, particle size reduction technologies, pharmaceutical salts, prodrugs, the solid-state alternation technique, soft gel technology, drug nanocrystals, solid dispersion methods, crystal engineering techniques and nanomorph technology. This review mainly describes several other advanced methodologies for solubility and bioavailability enhancement, such as crystal engineering, micronization, solid dispersions, nano sizing, the use of cyclodextrins, solid lipid nanoparticles, colloidal drug delivery systems and drug conjugates, referring to a number of appropriate research reports.

19 January 2021 in Macromolecular Bioscience
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Journal Article
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Arvind Singh ChandelArvind Singh Chandel
Arvind Singh Chandel
ASAtsushi Shimizu
Atsushi Shimizu
KHKiyoshi Hasegawa
Kiyoshi Hasegawa
TITaichi Ito
Taichi Ito

1 February 2018 in Journal of Hazardous Materials
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Journal Article
Closed access
ABAnupam Bera
Anupam Bera
JTJaladhi S. Trivedi
Jaladhi S. Trivedi
SKSweta Binod Kumar
Sweta Binod Kumar
Arvind Singh ChandelArvind Singh Chandel
Arvind Singh Chandel
SHSoumya Haldar
Soumya Haldar
SJSuresh K. Jewrajka
Suresh K. Jewrajka

27 January 2016 in ACS Applied Materials & Interfaces
Verified
Journal Article
Closed access
Arvind Singh ChandelArvind Singh Chandel
Arvind Singh Chandel
CKChinta Uday Kumar
Chinta Uday Kumar
SJSuresh Kumar Jewrajka
Suresh Kumar Jewrajka

9 November 2023 in International Journal of Biological Macromolecules
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Journal Article
Closed access
MPMeenakshi Paswan
Meenakshi Paswan
Arvind Singh ChandelArvind Singh Chandel
Arvind Singh Chandel
NMNaved I. Malek
Naved I. Malek
BDBharat Z. Dholakiya
Bharat Z. Dholakiya