2013
DOI: 10.3109/03639045.2013.814060
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Evaluation of biodegradable polyester-co-lactone microparticles for protein delivery

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Cited by 4 publications
(7 citation statements)
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“…2; Trace C). In addition, the reduced PGA-co-PDL peaks intensities was attributed to the processing steps and was also reported in our previous study using PGA-co-PDL encapsulated α-chymotrypsin and with PLGA nanoparticles entrapped cyclosporine (Tawfeek et al, 2014;Wagh and Apar, 2014). PGA-co-PDL/Eudragit MPs loaded IND (1:1.5 wt/wt ratio) showed complete disappearance of PGA-co-PDL characteristic peaks ( Fig.1; Trace D) which was attributed to the efficient coating of Eudragit L-100-55 around PGA-co-PDL particles.…”
Section: Pga-co-pdl Microparticle/eudragit Characterisationsupporting
confidence: 86%
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“…2; Trace C). In addition, the reduced PGA-co-PDL peaks intensities was attributed to the processing steps and was also reported in our previous study using PGA-co-PDL encapsulated α-chymotrypsin and with PLGA nanoparticles entrapped cyclosporine (Tawfeek et al, 2014;Wagh and Apar, 2014). PGA-co-PDL/Eudragit MPs loaded IND (1:1.5 wt/wt ratio) showed complete disappearance of PGA-co-PDL characteristic peaks ( Fig.1; Trace D) which was attributed to the efficient coating of Eudragit L-100-55 around PGA-co-PDL particles.…”
Section: Pga-co-pdl Microparticle/eudragit Characterisationsupporting
confidence: 86%
“…5C). Similar results have been reported by Tawfeek et al (Tawfeek et al, 2014), using high concentrations of SSG in FDTs containing itopride HCl significantly decreased the in vitro disintegration time (Tawfeek et al, 2015). Hence, it could be concluded that formulation 12SSG-5CF was considered an optimum formulation in terms of in vitro disintegration time as stated in the optimum time for disintegration for orodispersible tablets in European Pharmacopeia (pharmacopoeia, 2002).…”
Section: Optimizing the Fdtssupporting
confidence: 84%
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