2019
DOI: 10.1002/slct.201902739
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Synthesis, Characterization of a Baicalin‐Strontium(II) Complex and Its BSA‐Binding Activity

Abstract: Baicalin is one of the major bioactive constituents of Scutellaria baicalensis Georgi, possessed anti‐inflammation, antimicrobial and anticancer activity, has been attained extensive attention. In the present work, a new baicalin‐Sr(II) complex (Sr[baic]⋅3H2O) was synthesized to enhance its biological activity. A series of experiments were carried out to give the satisfying reaction conditions: pH=8.3 and the molar ratio of L:M ≤ 1:1. The obtained complex Sr[baic]⋅3H2O was characterized by IR, ES‐MS UV‐vis, at… Show more

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Cited by 4 publications
(4 citation statements)
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“…At the same time, the enthalpy and entropy change of micellization (ΔmicH and ΔmicS ) are calculated by Equations 18 and : trueΔmicH=RT(X1mlnf1m+()1-normalX1normalmlnf2m) trueΔmicS=(ΔmicH-ΔmicG)/T …”
Section: Resultsmentioning
confidence: 99%
“…At the same time, the enthalpy and entropy change of micellization (ΔmicH and ΔmicS ) are calculated by Equations 18 and : trueΔmicH=RT(X1mlnf1m+()1-normalX1normalmlnf2m) trueΔmicS=(ΔmicH-ΔmicG)/T …”
Section: Resultsmentioning
confidence: 99%
“…Baicalin has also been used to treat diarrheic piglets by inhibiting bacterial adhesion and inflammatory responses due to ETEC infection [ 20 , 21 ]. With electron-rich carbonyl and carboxyl groups, baicalin can complex with metal ions to result in higher bioactivity [ 22 ]. It has previously been shown that baicalin-zinc and baicalin-copper can enhance the antioxidant capacity and nutrient absorption of pigs [ 23 , 24 ].…”
Section: Discussionmentioning
confidence: 99%
“…[22] The binding capacity of the drug with the protein determines its pharmacodynamic properties like distribution, retention, excretion, and dosage frequency. [23][24][25] A large binding constant lessens free drug concentration in plasma and thus therapeutic effects would enhance. Drug toxicity dwindled with decreasing frequent use and increasing the binding with albumin protein.…”
Section: Introductionmentioning
confidence: 99%
“…Disulfide bonds organize the BSA single chain into nine loops for binding, while hydrogen bonds can easily be disrupted under the influence of chemical denaturants [22] . The binding capacity of the drug with the protein determines its pharmacodynamic properties like distribution, retention, excretion, and dosage frequency [23–25] . A large binding constant lessens free drug concentration in plasma and thus therapeutic effects would enhance.…”
Section: Introductionmentioning
confidence: 99%