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4 articles for “in vitro drug release”
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Formulation and Characterization of Polyhydroxyalkanoates Copolymer Nanoparticles for Controlled Drug Release
Abstract: The present study was focused on the formulation of polyhydroxyalkanoates copolymer nanoparticles (PHANPs) for in vitro controlled release of the drugs, viz. levofloxacin and amoxicillin. The PHANPs were synthesized by a triple emulsion method and conjugated with amoxicillin and levofloxacin to improve its remedial bioavailability. The PHANPs and drug conjugatedPHANPs were analysed using Scanning Electron Microscopy (SEM), Fourier Transform Infrared (FTIR) spectroscopy and X-Ray Diffraction (XRD). The cell viability % …
Published in International journal of Nanobiotechnology · Vol. 6, Issue 2, 2020 · pp. 1–11 Read article
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In-Vitro Evaluation of Control Release of Drug with Carbon Based Nanomaterials
Abstract: Nanomaterials have been introduced as a novel & interesting materials due to their advance properties & their use in nanotechnology applications like nano-sensors, nano-chips, control & targeted drug delivery, diagnosis, gene therapy. These all possibilities are due to their physico-chemical & multifunctional biological characteristics. In medicine, control release of drug is a factor to reduce dosage form in revert reduce side effects. In this work, nanomaterials are using as a …
Published in International journal of Nanobiotechnology · Vol. 1, Issue 1-2, 2015 · pp. 14–18 Read article
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Nanotechnology Based Drug Delivery System in Tuberculosis: Review
Abstract: From near the beginning centuries to present life Tuberculosis remains the world-wide disease without any limitations. In the other hand, in some cases in the infected individuals the disease remains in a dormant state. In this stage the treatment is hard as the lipid mycobacterial wall is thick & the delivery of drug inside the bacterial cell is difficult. Due to this new face of TB it becomes the major …
Published in International journal of Nanobiotechnology · Vol. 3, Issue 2, 2017 · pp. 14–24 Read article
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Formulation Development and Evaluation of Mouth Dissolving Tablets of Cilnidipine
Abstract: Orodispersible tablets (ODT) are tablets that dissolve quickly or disintegrate in the oral cavity without the need for water. In this study, orodispersible tablets containing Cilnidipine (an antihypertensive agent) were formulated by direct compression method to improve the safety and efficacy of the drug molecules and achieve better patient compliance. Cilnidipine is an antihypertensive drug and acts as a calcium channel blocker. The aim of this study was to develop …
Published in International Journal of Analytical and Applied Chemistry · Vol. 9, Issue 2, 2023 · pp. 38–44 Read article