Fabrication, characterization and cytotoxicity studies of ionically cross-linked docetaxel loaded chitosan nanoparticles

Jain, Ankit; Thakur, Kanika; Sharma, Gajanand; Kush, Preeti; Jain, Upendra Kumar

doi:10.1016/j.carbpol.2015.10.012

Cited by 103 publications

(54 citation statements)

References 47 publications

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“…These findings are somewhat in concordance with the studies which report that cross linking density decreases, and thus particle size increases, as a result of increasing drug concentration, which leads to decreasing chitosan amount in the dribble of the same volume (Bodmeier, Paeratakul, 1989;Wan, Lim, Soh, 1994;Jain et al, 2016;Joseph, Sangeetha, Gomathi, 2016).…”

Section: The Effect Of Drug Concentrationsupporting

confidence: 81%

“…However, when the chitosan concentration was 3% (F11), the particle size increased significantly to 1086 μm (p<0.05). These findings were attributed to the fact that TPP amount proved insufficient due to the increase in the chitosan viscosity and decrease in the cross linking density due to its being incapable of diffusing into the particles (Shirashi, Imai, Otagiri, 1993, Gan et al, 2005Jain et al, 2016;Joseph, Sangeetha, Gomathi, 2016).…”

Section: The Effect Of Polymer Concentrationmentioning

confidence: 98%

“…On the other hand, when microspheres were prepared by using TPP with 1% (F1) and 2% (F2) ratios in the external phase, it was found out that particle size decreases as TPP ratios increase (Table III) (Jain et al, 2016). Therefore, TPP concentration was set to 2% in this study.…”

Section: Crosslinking Agent Effectmentioning

confidence: 99%

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Investigation of the parameters affecting the release of flurbiprofen from chitosan microspheres

Tilkan

Özdemir

2018

Braz. J. Pharm. Sci.

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Flurbiprofen (FLB), a NSAID, widely used for preventing pain generally for arthritis or dental problems. In this study, FLB loaded chitosan microspheres were prepared by ionotropic gelation method. In this method, microspheres were formed by dropping chitosan solutions containing FLB into sodium alginate solutions including sodium tripolyphosphate (TPP). A variety of formulation parameters like drug:polymer ratio, drug concentration, polymer's molecular weight, polymer concentration, pH and the concentration of TPP solutions, drying method and stirring time were analyzed. The dissolution studies were performed in a shaking water bath in pH 7.4 phosphate buffer saline (PBS) at 37 °C. Laser diffractometer was used for particle size analysis, and scanning electron microscope (SEM) was used for morphological properties. Drug loading and loading efficiency were calculated by using UV spectrophotometer. The particles obtained were spherical with 0.7-1.3 mm size range, and the loading efficiency was approximately 21-79%. The dissolution studies conducted revealed that drug:polimer ratio and the polymer type and concentration affected the drug release from microspheres. It was observed that increasing the polymer concentration, polymer's molecular weight and TPP concentration decreased the FLB release from microspheres, which was according to Higuchi kinetics.

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Section: The Effect Of Drug Concentrationsupporting

confidence: 81%

Section: The Effect Of Polymer Concentrationmentioning

confidence: 98%

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Investigation of the parameters affecting the release of flurbiprofen from chitosan microspheres

Tilkan

Özdemir

2018

Braz. J. Pharm. Sci.

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“…Ltd., Mumbai, India) at IMTECH, Chandigarh, India. The mean size was directly obtained from the instrument software (22).…”

Section: Micromeriticsmentioning

confidence: 99%

Delivery of Thermoresponsive-Tailored Mixed Micellar Nanogel of Lidocaine and Prilocaine with Improved Dermatokinetic Profile and Therapeutic Efficacy in Topical Anaesthesia

et al. 2016

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The topical delivery of local anaesthetics has always been a difficult task due to the limited percutaneous absorption of local anaesthetic drugs across the various barriers of the skin. In this pursuit, a thermoresponsive mixed micellar nanogel (MMNG) system of lidocaine and prilocaine has been attempted in the current piece of work. The system relies on the ability to alter its phase state (sol-to-gel) for feasibility of the topical application in response to change in temperature. The composition of MMNG entails majorly of Pluronic® F127 and Tween 80 in a fixed combination so as to provide the desired thermoreversibility for the skin application. The gels were optimized with respect to phase transition temperature (T ), turbidity and viscosity. The optimized systems were then characterized for particle size, spreadability, syringeability, bioadhesive strength, ex vivo skin permeation, retention and dermatokinetic studies. The skin compatibility revealed that no histological changes were observed for optimized formulation, while the conventional system showed changes in the skin-tissues. Further, the enhanced intensity of anaesthetic effect was noted in an in vivo rabbit model and tail flick model in mice. The overall results suggest that the prepared MMNG system possesses the potential in providing an efficacious, safe and acceptable alternative therapeutic system for topical anaesthesia.

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“…A drop of diluted sample was placed on the surface of carbon-coated copper grid and stained with a drop of (1%, w/v) aqueous solution of phosphotungstic acid. The thin film formed on the surface of copper grid was viewed under the microscope at a suitable magnification (Jain et al, 2016).…”

Section: Morphology and Structure Of Vesiclesmentioning

confidence: 99%

Novel elastic membrane vesicles (EMVs) and ethosomes-mediated effective topical delivery of aceclofenac: a new therapeutic approach for pain and inflammation

et al. 2016

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Context: Aceclofenac (ACE) is a systematically designed drug, developed to circumvent the concerns associated with diclofenac. But ACE is also associated with non-steroidal antiinflammatory drug (NSAIDs)-tagged side effects, although of decreased amplitude. Objective: The present study aims to develop phospholipid-based vesicles (elastic membrane vesicles; EMV and ethosomes) loaded with ACE and explore their potential in topical delivery. Methods: Elastic membrane vesicles (EMVs) were prepared by thin-film hydration method and ethosomes by cold method. The composition of both the vesicular systems was selected on the basis of vesicle density and drug entrapment. The developed systems were characterized for micromeritics, surface charge, drug entrapment, and morphology. Ex vivo permeation and retention studies on Laca mice skin were performed. In vivo pharmacodynamic evaluation was performed by tail-flick method and carrageenan-induced rat paw-edema model. During stability studies, percent drug leakage was studied. Results: The selected ratios of phospholpid:drug:stearylamine for EMVs and ethosomes were 8:1:1 and 3:1:1, respectively. The ethosomes were found to offer more vesicle density, drug loading, and deformability index as compared with that of EMVs. The drug permeation and the retention offered by both the vesicular systems were superior to that of the conventional cream; however, performance of ethosomes superseded that of EMVs. The phospholipid-based vesicles were found to be well tolerated on mice skin. Although, the in vivo performance of ethosomes was found to be better than that of EMVs in both the studied models. Conclusion: The phospholipid-based vesicular systems, especially, ethosomes can be a promising tool to enhance the delivery and safety of ACE by topical route.

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Fabrication, characterization and cytotoxicity studies of ionically cross-linked docetaxel loaded chitosan nanoparticles

Cited by 103 publications

References 47 publications

Investigation of the parameters affecting the release of flurbiprofen from chitosan microspheres

Investigation of the parameters affecting the release of flurbiprofen from chitosan microspheres

Delivery of Thermoresponsive-Tailored Mixed Micellar Nanogel of Lidocaine and Prilocaine with Improved Dermatokinetic Profile and Therapeutic Efficacy in Topical Anaesthesia

Novel elastic membrane vesicles (EMVs) and ethosomes-mediated effective topical delivery of aceclofenac: a new therapeutic approach for pain and inflammation

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