2007
DOI: 10.1016/j.ijpharm.2007.01.046
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Optimized preparation of daidzein-loaded chitosan microspheres and in vivo evaluation after intramuscular injection in rats

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Cited by 35 publications
(32 citation statements)
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“…The incubation times for these groups were 1, 3, 6, 12, 24 h respectively, while the last group served as control without mixing with microspheres. The microsphere concentration (10mg/10mL blood) was chosen depending on previous studies [17]. At the end of the incubation time of each group, the blood was filtered from the microspheres by decantation, and the blood was examined for the following parameters:…”
Section: Resultsmentioning
confidence: 99%
“…The incubation times for these groups were 1, 3, 6, 12, 24 h respectively, while the last group served as control without mixing with microspheres. The microsphere concentration (10mg/10mL blood) was chosen depending on previous studies [17]. At the end of the incubation time of each group, the blood was filtered from the microspheres by decantation, and the blood was examined for the following parameters:…”
Section: Resultsmentioning
confidence: 99%
“…Among the suitable degradable polymers is chitosan, which is a potential useful as pharmaceutical material for transdermal patch development owing to its good biocompatibility and low toxicity (16,17). Chitosan is the most abundant basic biopolymer based on a linear amino polysaccharide of D-glucosamine and N-acetyl-D-glucosamine being obtained by the partial deacetylation of natural polymer chitin, the major compound of exoskeletons in crustaceans such as crabs, prawns, lobsters, the cuticles of insects, and the cell walls of fungi (16,18).…”
Section: Introductionmentioning
confidence: 99%
“…Thus, the chitosan is soluble after stirring in acids such as acetic, nitric, hydrochloric, perchloric, and phosphoric, but it is insoluble in water, organic solvents, and aqueous bases (19,20). The degradation products of chitosan are nontoxic, nonimmunogenic, and noncarcinogenic making it safe for drug delivery application (17). Recently, chitosan is used to control release and also prepare as hydrogels in transdermal drug delivery systems of many drugs such as repaglinide (8), ciprofloxacin hydrochloride (21), warfarin (22), salicylic acid (23), prednisolone (24), and rhodamine B (25).…”
Section: Introductionmentioning
confidence: 99%
“…Another approach is using injectable microbeads, which combine the advantages of high surface areato-volume ratio and more controlled cross-linking efficiency. The use of implant configuration as a basis for producing more potent constructs for tissue engineering and induction of angiogenesis have been inadvertently underestimated and still remain poorly studied for lack of good experimental tools that can continuously and noninvasively monitor the fate of the implants in vivo.Various invasive techniques have been described for documenting implant resorption in vivo; however, these techniques do not provide detailed information about the in situ integration process and require destructive analysis of postmortem sections (13,(16)(17)(18). With the optimization of a hydrogel scaffold requiring more information of the transient steps of integration, techniques to continuously monitor the degradation of a scaffold using fluorescence labeling have been described (15,19,20).…”
mentioning
confidence: 99%
“…Various invasive techniques have been described for documenting implant resorption in vivo; however, these techniques do not provide detailed information about the in situ integration process and require destructive analysis of postmortem sections (13,(16)(17)(18). With the optimization of a hydrogel scaffold requiring more information of the transient steps of integration, techniques to continuously monitor the degradation of a scaffold using fluorescence labeling have been described (15,19,20).…”
mentioning
confidence: 99%