Vinod Gaikwad

Dr. Vinod Gaikwad

orcid

Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

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

Representative Publications

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1 January 2009 in Asian Journal of Pharmaceutics
Verified
Journal Article
Closed access
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NJNamdeoR Jadhav
NamdeoR Jadhav
VGVinod Gaikwad
Vinod Gaikwad
KNKarthikJ Nair
KarthikJ Nair
HKHanmantraoM Kadam
HanmantraoM Kadam
Glass transition temperature (Tg) is an important tool used to modify physical properties of drug and polymer molecules. Tg is shown by certain crystalline as well as amorphous solids. During the process of heating, some solid gets melted and if quench cooled, instead of crystallizing, gets converted to amorphous solid form appearing as that of glass. This glass formation is seen because of the dynamic arrest of molecules forming a disordered state at Tg. The molecules/atoms in glassy state are subject to only vibration and not translational and rotational motion. Mainly, at Tg, conversion of glassy (vitrified, amorphous) solid to rubbery (viscous liquid) takes place. Numerous factors like structural change in molecules, cooling rate and incorporation of additives alter the Tg. Techniques like differential scanning calorimetry, elastic modulus, broad-line NMR are used to measure the Tg of substances. The change in Tg has been carried out to improve dissolution and bioavailability, processing and handling qualities of the material.

11 July 2023 in Drug Discovery Today
Verified
Journal Article
Closed access
RPRuchika S. Patil
Ruchika S. Patil
SKSamruddhi B. Kulkarni
Samruddhi B. Kulkarni
VGVinod Gaikwad
Vinod Gaikwad

1 January 2019
Verified
Book Chapter
Closed access
VGVinod Gaikwad
Vinod Gaikwad
PCPrafulla B. Choudhari
Prafulla B. Choudhari
NBNeela M. Bhatia
Neela M. Bhatia
MBManish S. Bhatia
Manish S. Bhatia

1 October 2013 in Saudi Pharmaceutical Journal
Verified
Journal Article
Open access
VGVinod Gaikwad
Vinod Gaikwad
MBManish S. Bhatia
Manish S. Bhatia
Drug release from various polymers is generally governed by the type of polymer/s incorporated in the formulation and mechanism of drug release from polymer/s. A single polymer may show one or more mechanisms of drug release out of which one mechanism is majorly followed for drug release. Some of the common mechanisms of drug release from polymers were, diffusion, swelling, matrix release, leaching of drug, etc. Mechanism or rate of drug release from a polymer or a combination of polymers can be predicted by using different computational methods or models. These models were capable of predicting drug release from its dosage form in advance without actual formulation and testing of drug release from dosage form. Quantitative structure-property relationship (QSPR) is an important tool used in the prediction of various physicochemical properties of actives as well as inactives. Since last several decades QSPR has been applied in new drug development for reducing the total number of drugs to be synthesized, as it involves a selection of the most desirable compound of interest. This technique was also applied in predicting in vivo performance of drug/s for various parameters. QSPR serves as a predictive tool to correlate structural descriptors of molecules with biological as well as physicochemical properties. Several researchers have contributed at different extents in this area to modify various properties of pharmaceuticals. The present review is focused on a study of different polymers that influence the transportability profiles of drugs along with the application of QSPR either to study different properties of polymers that regulate drug release or in predicting drug transportability from different polymer systems used in formulations.

25 August 2023 in ADMET and DMPK
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Journal Article
Open access
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Smita KumbharSmita Kumbhar
Smita Kumbhar
RKRupali Khairate
Rupali Khairate
MBManish Bhatia
Manish Bhatia
PCPrafulla Choudhari
Prafulla Choudhari
VGVinod Gaikwad
Vinod Gaikwad
Background and purpose: Wound healing is a biological process that can be difficult to manage clinically. In skin wound healing, the interaction of many cells, growth factors, and cytokines reveals an outstanding biological function mechanism. Wound healing that occurs naturally restores tissue integrity, however, it is usually restricted to wound repair. Curcumin synthesised in a chitosan matrix can be used to heal skin sores. Experimental approach: The ionotropic gelation procedure required crosslinking chitosan with a tripoly­phos­phate (TPP) crosslinker to generate curcumin nanoparticles encapsulated in chitosan. Key results: The nanoparticles were between 200 and 400 nm in size, with a strong positive surface charge and good entrapment efficacy, according to SEM and TEM investigations. Curcumin and chitosan compatibility was investigated using FTIR spectroscopy. All batches showed consistent drug release, with the F5 batch having the highest curcumin release, at 75% after 16 hours. On L929 cells, scratch assays were utilised to assess wound healing. Wound closure with widths of 59 and 65 mm with curcumin and 45 and 78 mm with curcumin-loaded chitosan nanoparticles was seen after 24 and 48 hours of examination. Conclusions: According to the findings, prepared curcumin chitosan nanoparticles are beneficial in healing skin damage.

26 July 2019 in AAPS PharmSciTech
Verified
Journal Article
Closed access
AKAjit S. Kulkarni
Ajit S. Kulkarni
AKAmit J. Kasabe
Amit J. Kasabe
MBManish S. Bhatia
Manish S. Bhatia
NBNeela M. Bhatia
Neela M. Bhatia
VGVinod Gaikwad
Vinod Gaikwad