2007
DOI: 10.1002/jps.20730
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Novel Biopolymers as Implant Matrix for the Deliveryof Ciprofloxacin: Biocompatibility, Degradation, and In Vitro Antibiotic Release

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Cited by 15 publications
(8 citation statements)
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“…Rosin biomaterias have excellent biocompatibility and degradation features, and film-forming ability (Fulzele et al 2003). They show potential as components in film-based drug delivery systems and dosage technology (Satturwar et al 2005;Fulzele et al 2007). …”
Section: Pine Resinmentioning
confidence: 99%
See 1 more Smart Citation
“…Rosin biomaterias have excellent biocompatibility and degradation features, and film-forming ability (Fulzele et al 2003). They show potential as components in film-based drug delivery systems and dosage technology (Satturwar et al 2005;Fulzele et al 2007). …”
Section: Pine Resinmentioning
confidence: 99%
“…It is a brittle, transparent, glassy solid produced by heating fresh liquid resin to vaporize the volatile liquid terpene components. Rosin and rosin derivatives have been pharmaceutically evaluated as microencapsulating materials and as anhydrous binding agents in tablets (Fulzele et al 2002(Fulzele et al , 2007Pathak and Dorle 1990;Sahu et al 1999;Satturwar et al 2004;Lee et al 2005). Rosin biomaterias have excellent biocompatibility and degradation features, and film-forming ability (Fulzele et al 2003).…”
Section: Pine Resinmentioning
confidence: 99%
“…Although a number of research articles have been published on the controlled release of antibiotics given systemically or as postoperative implants, few reports are associated with controlled release of antibiotics following pulmonary delivery [130,[202][203][204]. One such study used the encapsulation of nafcillin and levofloxacin in PLGA nanoparticles coated with calcium phosphate, to achieve controlled release of the antibiotics.…”
Section: Mycobacterium Smegmatismentioning
confidence: 99%
“…Previous studies have examined the in vitro/in vivo correlation (IVIVC) for various other drug delivery systems, suggesting that the IVIVC varies with each compound and polymer matrix (Wang et al 1996). It is hypothesized that this is due in part to the foreign body response (Fulzele et al 2007). As other researchers have concluded, more sophisticated in vitro models mimicking drug release under in vivo conditions are necessary for parenteral depot formulations, specifically for risperidone implant configurations (Schliecker et al 2004).…”
Section: Critical Issues and Future Directionsmentioning
confidence: 99%