Insights into the temperature and concentration dependent studies of the Anti-diabetic drug in aqueous binary and ternary (water +sucrose) mixtures at body temperature

Thermodynamic and compressibility studies together with biological studies play an important role in the effective design and development of drug. In the current study, various drug-molecular interactions have been studied from thermophysical properties. The experimental density(ρ) and speed of soun...

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Autores principales: Ankita S. Chandak, Sangesh P. Zodape
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Lenguaje:EN
Publicado: Elsevier 2021
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Acceso en línea:https://doaj.org/article/c0c7116eb47e49ea846598a3a6339f17
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spelling oai:doaj.org-article:c0c7116eb47e49ea846598a3a6339f172021-11-10T04:43:46ZInsights into the temperature and concentration dependent studies of the Anti-diabetic drug in aqueous binary and ternary (water +sucrose) mixtures at body temperature2667-022410.1016/j.chphi.2021.100050https://doaj.org/article/c0c7116eb47e49ea846598a3a6339f172021-12-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2667022421000396https://doaj.org/toc/2667-0224Thermodynamic and compressibility studies together with biological studies play an important role in the effective design and development of drug. In the current study, various drug-molecular interactions have been studied from thermophysical properties. The experimental density(ρ) and speed of sound(u) measurements for anti-diabetic drug Metformin hydrochloride (M.HCl) in binary as well as in ternary mixtures have been reported within the concentration range of 0.03–0.15 mol.kg−1 at various temperatures (305.15, 310.15 and 315.15 K) and atmospheric pressure. Various parameters like apparent molar volume of solute (Vϕ) and apparent molar compressibility of solute (KS,ϕ), limiting apparent molar volume of solute (Vϕ0), limiting apparent molar compressibility of solute (KS,ϕ0) and hydration number (nh) have been measured for binary (M.HCl + water) as well as ternary (M.HCl + Sucrose + Water) systems systematically using the experimentally measured ρ and u data. Further transfer volume (ΔtrVϕ0) of M.HCl from water to aqueous sucrose solutions have been measured at different temperatures. The hydration behavior of M.HCl has been understood from the obtained values of hydration number for studied systems at various temperatures. All the experimental results have been analysed in the light of various interactions among molecules of solvent and solute respectively.Ankita S. ChandakSangesh P. ZodapeElsevierarticleMetformin hydrochlorideSucroseApparent molar volumeApparent molar compressibilityHydration numberPhysicsQC1-999ChemistryQD1-999ENChemical Physics Impact, Vol 3, Iss , Pp 100050- (2021)
institution DOAJ
collection DOAJ
language EN
topic Metformin hydrochloride
Sucrose
Apparent molar volume
Apparent molar compressibility
Hydration number
Physics
QC1-999
Chemistry
QD1-999
spellingShingle Metformin hydrochloride
Sucrose
Apparent molar volume
Apparent molar compressibility
Hydration number
Physics
QC1-999
Chemistry
QD1-999
Ankita S. Chandak
Sangesh P. Zodape
Insights into the temperature and concentration dependent studies of the Anti-diabetic drug in aqueous binary and ternary (water +sucrose) mixtures at body temperature
description Thermodynamic and compressibility studies together with biological studies play an important role in the effective design and development of drug. In the current study, various drug-molecular interactions have been studied from thermophysical properties. The experimental density(ρ) and speed of sound(u) measurements for anti-diabetic drug Metformin hydrochloride (M.HCl) in binary as well as in ternary mixtures have been reported within the concentration range of 0.03–0.15 mol.kg−1 at various temperatures (305.15, 310.15 and 315.15 K) and atmospheric pressure. Various parameters like apparent molar volume of solute (Vϕ) and apparent molar compressibility of solute (KS,ϕ), limiting apparent molar volume of solute (Vϕ0), limiting apparent molar compressibility of solute (KS,ϕ0) and hydration number (nh) have been measured for binary (M.HCl + water) as well as ternary (M.HCl + Sucrose + Water) systems systematically using the experimentally measured ρ and u data. Further transfer volume (ΔtrVϕ0) of M.HCl from water to aqueous sucrose solutions have been measured at different temperatures. The hydration behavior of M.HCl has been understood from the obtained values of hydration number for studied systems at various temperatures. All the experimental results have been analysed in the light of various interactions among molecules of solvent and solute respectively.
format article
author Ankita S. Chandak
Sangesh P. Zodape
author_facet Ankita S. Chandak
Sangesh P. Zodape
author_sort Ankita S. Chandak
title Insights into the temperature and concentration dependent studies of the Anti-diabetic drug in aqueous binary and ternary (water +sucrose) mixtures at body temperature
title_short Insights into the temperature and concentration dependent studies of the Anti-diabetic drug in aqueous binary and ternary (water +sucrose) mixtures at body temperature
title_full Insights into the temperature and concentration dependent studies of the Anti-diabetic drug in aqueous binary and ternary (water +sucrose) mixtures at body temperature
title_fullStr Insights into the temperature and concentration dependent studies of the Anti-diabetic drug in aqueous binary and ternary (water +sucrose) mixtures at body temperature
title_full_unstemmed Insights into the temperature and concentration dependent studies of the Anti-diabetic drug in aqueous binary and ternary (water +sucrose) mixtures at body temperature
title_sort insights into the temperature and concentration dependent studies of the anti-diabetic drug in aqueous binary and ternary (water +sucrose) mixtures at body temperature
publisher Elsevier
publishDate 2021
url https://doaj.org/article/c0c7116eb47e49ea846598a3a6339f17
work_keys_str_mv AT ankitaschandak insightsintothetemperatureandconcentrationdependentstudiesoftheantidiabeticdruginaqueousbinaryandternarywatersucrosemixturesatbodytemperature
AT sangeshpzodape insightsintothetemperatureandconcentrationdependentstudiesoftheantidiabeticdruginaqueousbinaryandternarywatersucrosemixturesatbodytemperature
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