2022
DOI: 10.1016/j.ejps.2022.106133
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Improved solubility of lornoxicam by inclusion into SBA-15: Comparison of loading methods

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Cited by 9 publications
(6 citation statements)
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“…Summing up, it can be concluded that the dose of 25 kGy causes little changes in the physicochemical properties of the drug, in contrast to the dose of 400 kGy, which causes decomposition of the drug. The HPLC method was used to determine the content of DC and AC before and after irradiation, which was validated according to the ICH guidelines [ 27 ]. In the chromatogram of the AC before irradiation, one peak with a retention time of 12.26 min, while for DC two signals with retention times of 1.75 min and 11.46 min were observed.…”
Section: Resultsmentioning
confidence: 99%
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“…Summing up, it can be concluded that the dose of 25 kGy causes little changes in the physicochemical properties of the drug, in contrast to the dose of 400 kGy, which causes decomposition of the drug. The HPLC method was used to determine the content of DC and AC before and after irradiation, which was validated according to the ICH guidelines [ 27 ]. In the chromatogram of the AC before irradiation, one peak with a retention time of 12.26 min, while for DC two signals with retention times of 1.75 min and 11.46 min were observed.…”
Section: Resultsmentioning
confidence: 99%
“…Within the concentration range from 0.5038 × 10 −4 to 6.0456 × 10 −4 g/mL for AC and 0.5014 × 10 −4 to 6.0168 × 10 −4 g/mL for DC the method was linear, characterized by a very good correlation coefficient (r = 0.9975–0.9978) and high precision (RSD = 1.07–1.15%). The method was validated according to the Guidelines of the International Conference on Harmonization [ 27 ]. The content of DC and AC was calculated by reference to the standard.…”
Section: Resultsmentioning
confidence: 99%
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“…Our results are in line with previous reports. 7,68 For 24 h incubation, the toxic effect of Irinotecan, when adsorbed onto NPs pore framework, is amplified compared to Irinotecan in solution. Although the Irinotecan concentrations provided by each of the NPs suspensions are the same (10 µg mL −1 ), Iri@SBA-15 cytotoxicity (Fig.…”
Section: Cell Viabilitymentioning
confidence: 99%
“…Lornoxicam is a non-steroidal anti-inflammatory drug (NSAID) having low aqueous solubility and high permeability through biological membranes leading to low bioavailability [1]. Several approaches such as complexation with cyclodextrins, solid dispersion, emulsion and cocrystallization are employed to enhance the solubility and subsequently bioavailability of active pharmaceutical ingredients (APIs).…”
Section: Introductionmentioning
confidence: 99%