2020
DOI: 10.1016/j.heliyon.2020.e05365
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In situ ophthalmic gel forming systems of poloxamer 407 and hydroxypropyl methyl cellulose mixtures for sustained ocular delivery of chloramphenicole: optimization study by factorial design

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Cited by 46 publications
(33 citation statements)
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References 25 publications
(34 reference statements)
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“…In vitro diffusion study of the phenolic compounds of the prepared formulations was performed using a Franz diffusion cell [ 83 ]. The results of the tests confirmed the data obtained by other scientists—the released amounts of the active compounds depended on the amount of gelling agent [ 35 , 46 ]. The greater the concentration of the gelling agent in the formulation, the slower the rate of release of the active compounds.…”
Section: Discussionsupporting
confidence: 86%
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“…In vitro diffusion study of the phenolic compounds of the prepared formulations was performed using a Franz diffusion cell [ 83 ]. The results of the tests confirmed the data obtained by other scientists—the released amounts of the active compounds depended on the amount of gelling agent [ 35 , 46 ]. The greater the concentration of the gelling agent in the formulation, the slower the rate of release of the active compounds.…”
Section: Discussionsupporting
confidence: 86%
“…In view of the fact that the bioavailability of eye drops can be improved by increased precorneal residence time [ 60 ], in situ gels were chosen for production. In situ gels, due to their viscosity, slow down the speed of drug elimination from the eye [ 46 ]. An important step in the formulation of in situ gels is the choice of excipients, which could ensure the stability of preparations without changing the activity of bioactive ingredients, and be non-irritant—especially when used locally on the surface of the eye [ 61 , 62 ].…”
Section: Discussionmentioning
confidence: 99%
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