2020
DOI: 10.1002/mawe.201900163
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Antibiotic drug release behavior of poly (vinyl alcohol)/sodium alginate hydrogels

Abstract: Poly (vinyl alcohol)/sodium alginate hydrogels were prepared by freeze‐thaw followed by calcium ion crosslinking. Chloramphenicol release behavior from the poly (vinyl alcohol)/sodium alginate hydrogels in mimic conditions of gastrointestinal tract was examined. The effects of composition, number of freeze‐thaw cycles and calcium ion concentration on drug release process were investigated. The results showed that the cumulative release amount of chloramphenicol from the hydrogels (crosslinked through 4 freeze‐… Show more

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Cited by 26 publications
(19 citation statements)
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“…In recent studies, antimicrobial CAM was encapsulated in nonelectroresponsive polymeric carriers for release. [ 26–28 ] For example, CAM‐loaded polycaprolactone (PCL) nanofibers and, especially, PCL‐ polyethylene oxide (PEO) and microfiber exhibited a very fast release in PBS, reaching in 1 h more than 30% and 90%, respectively. [ 26 ] The difference between such two systems was attributed to the hydrophobic and hydrophilic nature of PCL and PCL‐PEO fibers, respectively.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…In recent studies, antimicrobial CAM was encapsulated in nonelectroresponsive polymeric carriers for release. [ 26–28 ] For example, CAM‐loaded polycaprolactone (PCL) nanofibers and, especially, PCL‐ polyethylene oxide (PEO) and microfiber exhibited a very fast release in PBS, reaching in 1 h more than 30% and 90%, respectively. [ 26 ] The difference between such two systems was attributed to the hydrophobic and hydrophilic nature of PCL and PCL‐PEO fibers, respectively.…”
Section: Resultsmentioning
confidence: 99%
“…In any case, the strength of the interaction between CAM and such polymers was significantly weaker than with PEDOT. Similarly, the release of CAM loaded in poly(vinyl alcohol)/sodium alginate hydrogels was very high, independently of the ratio between such two polymers, reaching more than 50% in less than 3 h. [ 27 ] Similarly, CAM was easily released from both loaded amorphous calcium phosphate and hydroxyapatite nanoparticles in the simple physiological PBS medium. [ 28 ] Overall, these observations support the strength of CAM⋅⋅⋅PEDOT interactions.…”
Section: Resultsmentioning
confidence: 99%
“…Thus, releasing of chloramphenicol from the loaded КC/SA/K + hydrogel is achieved only at pH 4.1 and shown in Figure 9. It is clear that the released drug quantity reached a constant value after about 3 hours, which can be interpreted in terms of the beaded hydrogel structure as well as the repulsive electrostatic interactions between the protonated acidic groups in the formed gel structure at pH 4.1 and the drug molecules that ultimately facilitate the releasing of such drug 51,52 …”
Section: Resultsmentioning
confidence: 99%
“…Polymer hydrogels evaluated were blends of poly­(vinyl alcohol) (PVA), sodium alginate (Alg), and chitosan (Ch). Cross-linking agents included CaCl 2 , boric acid, and NaOH . Data were collected in triplicate using a custom, student assembled pH measurement instrument called a “GelipHish” (build instructions in the Supporting Information (SI)).…”
Section: Discussionmentioning
confidence: 99%