Inventi Rapid - NDDS
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Journal Scope:
Quarterly published in print and online ‘Inventi Rapid/Impact: NDDS’ publishes high quality unpublished as well as high impact pre-published research and reviews catering to the needs of researchers and professionals. The journal covers all the areas under novel drug delivery systems. It welcomes articles pertaining to nano drug delivery systems; gastroretensive system, colonic drug delivery, bioadhesive and mucoadhesive systems; nasopulmonary drug delivery; ocular delivery; transdermal delivery, implants and inserts; protein and peptide delivery; manufacturing, quality control and regulatory aspects of NDDS, etc.
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NON-INVASIVE TRANSDERMAL DELIVERY OF LIPOSOMES BY WEAK ELECTRIC CURRENT
Non-invasive transdermal drug delivery (NTDD) system in a novel method of drug delivery. This review article describes the various delivery considerations and extraneous factors in developing a strategy to pursue an alternate route of administration for systemic delivery. This system is a technique that provides drug absorption via the skin. The system has many advantages over conventional adminis...
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FORMULATION AND EVALUATION OF FLOATING DRUG DELIVERY SYSTEM OF LOPERAMIDE HYDROCHLORIDE
The objective of the present study was to prepare the floating tablets of opioid-receptor agonist loperamide. Floating tablets constitute an innovative dosage form that overcome the problems of large frequency of dosing and provides a sustained action for a longer period of time. In the view of enhancing bioavailability an attempt has been made to prepare floating tablets and to know the effect of...
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FORMULATION OPTIMIZATION AND EVALUATION OF TASTE-MASKED CHEWABLE TABLET OF FEXOFENADINE HYDROCHLORIDE
The aim of the study was to mask the bitter taste of fexofenadine HCl using Eudragit E100 and prepared the chewable tablet. The taste masked granules of fexofenadine HCl were prepared by wet granulation method using pH sensitive, cationic copolymer eudragit E100 and pre-gelatinized starch as disintegrant and prepared into chewable tablet. Central composite design (CCD) was applied as an optimizati...
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FORMULATION AND EVALUATION OF NANOSTRUCTURED LIPID CARRIERS FOR ORAL DELIVERY OF CEFIXIME TRIHYDRATE
Nanostructured lipid carriers of cefixime trihydrate were prepared by hot melt micro emulsification method. The hot melt was prepared by heating the drug with a blend of solid lipid and liquid lipids: oleic and paraffin wax /bees wax is used as solid lipid and liquid lipids. FTIR studies of pure drug and formulations showed there was no significant change in the signal peaks of drugs; this indicat...
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FORMULATION AND CHARACTERIZATION OF LORATADINE PRONIOSOMAL GEL FOR TOPICAL DELIVERY
The present study was designed to investigate the potential of a novel class of vesicular system ‘proniosome’ as a carrier for transdermal delivery of loratadine proniosomal formulations. It was prepared by co-acervation phase separation method. The influence of factors like lipid concentration, cholesterol amount and drug content were studied. Span 60 was the most appropriate surfactant and y...
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FORMULATION OPTIMIZATION AND IN-VITRO RELEASE STUDIES OF ROSUVASTATIN CALCIUM LOADED CHITOSAN NANOPARTICLES
The rationale of the present study was to formulate, characterize and evaluate the polymeric nanoparticle of rosuvastatin calcium, a poorly water-soluble and low bioavailable drug with the intend of recuperating aqueous solubility consequently the dissolution rate. Rosuvastatin calcium (ROSCa) biodegradable polymeric nanoparticles were prepared by ionotropic gelation technique. Material and polyme...
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