[PDF] Top 20 FORMULATION AND IN VITRO EVALUATION OF SOLID DISPERSION OF β CYCLODEXTRIN COMPLEX OF GLIMEPIRIDE WITH POLOXAMER
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FORMULATION AND IN VITRO EVALUATION OF SOLID DISPERSION OF β CYCLODEXTRIN COMPLEX OF GLIMEPIRIDE WITH POLOXAMER
... containing β-Cyclodextrin, F13 to F15 correspond to preparations containing Poloxamer 188 and F16 to F18 correspond to preparation containing combination of β- Cyclodextrin and ... See full document
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ENHANCEMENT OF SOLUBILITY AND DISSOLUTION RATE OF ERLOTINIB HYDROCHLORIDE BY SOLID DISPERSION TECHNIQUE WITH POLOXAMER 188: PREPARATION AND IN VITRO EVALUATION
... Hydroxypropyl methylcellulose also known as methocel is a low viscosity water-soluble polymer. Polyethylene glycol is a polyether and also known as carbowax 19 . PL 188 is a non-ionic polymer containing hydrophilic and ... See full document
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FORMULATION AND COMPARITIVE IN VITRO EVALUATION OF ZOLPIDEM TARTRATE SOLID DISPERSION SUBLINGUAL TABLET
... as solid dispersion- sublingual (SDSL) tablets to maintain the desired plasma concentration of the ...The solid dispersion and physical mixtures of Zolpidem Tartrate in PEG-6000, PEG-4000 and ... See full document
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IN VITRO DISSOLUTION STUDY OF GLIMEPIRIDE FROM BINARY AND TERNARY SOLID DISPERSION FORMULATION
... the solid dispersion (SD) technique for dissolution enhancement of poorly water-soluble drugs 4 .... Glimepiride was selected as a model drug for dissolution enhancement studies in the present ... See full document
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Formulation Development and In-vitro Evaluation of Sustained Release Tablets of Carvedilol Solid Dispersion
... Carvedilol solid dispersion The solubility studies of the solid dispersions from formulation A1 to A6 were carried out in distilled ...of solid dispersion equivalent to 20mg of ... See full document
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ENHANCEMENT OF SOLUBILITY OF EFAVIRENZ EMPLOYING β -CYCLODEXTRIN, POLOXAMER 407 AND PVP K30: PHASE SOLUBILITY AND FACTORIAL STUDIES
... micronization, cyclodextrin complexation, use of surfactants and solubilizers, solid dispersion in water soluble and dispersible carriers, use of salts, prodrugs and polymorphs which exhibit high ... See full document
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FORMULATION AND IN VITRO EVALUATION OF SOLID DISPERSION OF FLUCONAZOLE
... preparing solid dispersions with using mannitol, urea, polyethylene glycol 6000, polyvinyl pyrrolidone K30 and ß-cyclodextrin as ...carrier. Solid dispersion of Fluconazole was prepared by ... See full document
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FORMULATION AND OPTIMIZATION OF SUBLINGUAL TABLETS OF TELMISARTAN
... Chitosan, Poloxamer (188, 407) Na.CMC and β‐cyclodextrin, PVP K30 were used for this ...K30, Poloxamer 407, and β‐cyclodextrin. Solid dispersion of Telmisartan With ... See full document
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A FACTORIAL STUDY ON FORMULATION DEVELOPMENT OF EFAVIRENZ TABLETS EMPLOYING Β CYCLODEXTRIN POLOXAMER 407 PVP K30
... solubilizers, solid dispersion and a few new emerging technologies such as cyclodextrin complexation, mucoadhesive microspheres, nano- particles, nanosuspensions, micro emulsion and self- emulsifying ... See full document
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Design, Development & Evaluation of Solid Dispersion Incorporated Transdermal Gel of Benzoyl Peroxide
... solubility. Solid Dispersion is an effective approach to improve its solubility and ...the solid dispersion incorporated trandermal gel of Benzoyl Peroxide can be improved with the use of ... See full document
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ENHANCEMENT OF DISSOLUTION RATE OF EFAVIRENZ EMPLOYING β -CYCLODEXTRIN, POLOXAMER 407 AND PVP K 30: A FACTORIAL STUDY
... micronization, cyclodextrin complexation, use of surfactants and solubilizers, solid dispersion in water soluble and dispersible carriers, use of salts, prodrugs and polymorphs which exhibit high ... See full document
6
Nanoparticle Formation of Puerarin-beta-Cyclodextrin Inclusion Complex Using SEDS: Dissolution Enhancement
... Drug release studies were performed in distilled water to evaluate the extent to which the loading process improved the water solubility of puerarin. Fig. 4 shows that in the same experimental conditions, after 5 min the ... See full document
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FORMULATION AND IN VITRO EVALUATION OF GASTRO RETENTIVE NON EFFERVESCENT TABLETS OF BALOFLOXACIN
... In-vitro dissolution studies : The release rate of Balofloxacin from floating tablet was determined using the United States Pharmacopoeia (USP) dissolution testing apparatus II. The dissolution test was performed ... See full document
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FORMULATION AND EVALUATION OF SOLID DISPERSION OF OLANZEPINE
... Palliative radiotherapy delivered to patients with locally advanced lung cancer who are not eligible for radical treatment or for patients with metastatic disease with symptoms such as b[r] ... See full document
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FORMULATION AND IN VITRO EVALUATION OF GASTRORETENTIVE BILAYER FLOATING TABLETS OF LOSARTAN POTASSIUM
... In vitro buoyancy studies and in vitro dissolution studies were performed in ...formulations, formulation BFT8 was found to be most promising formulation as it has shown most consistent drug ... See full document
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Title: ANTIEPILEPTIC DRUGS: TREATMENT IN ELDERLY PATIENTS. Author: Callegari C. *, Bianchi L., Vender S Keyword: Antiepileptic drugs, elderly patients, gabapentinPage No: 96-102Abstract: Introduction: This study aims to examine qualitatively the use of AEDs in a population of elderly patients in nursing homes, including the prescription of specialist and monitoring. Methods: This p revalence study was carried out in a state-founded nursing home providing assistance and rehabilitation for elderly people. The first objective of the study is to determine the prevalence of the use of antiepileptic drugs. The second objective is to study the monitoring the dosage modification from the time of admission of the patient until the end of the study. Results: In the period of time that we took into consideration 65 of 402 patient’s monitored patients had at least one anti-epileptic therapy (prevalence of 32%). The antiepileptic drug most prescribed was gabapentin with a frequency of 63.6%. Discussion: The prevalence use of AEDs has beeen 32%. The second objective concerns the drugs monitoring and it has also been achieved and shows how gabapentin is the most prescribed drug (53.8% psychiatrist) and was introduced mainly for anxiety disorders, psychosis, neuropathic pain and mood disorders. Keywords: Antiepileptic drugs, elderly patients, gabapentin Download PDF
... in range of 5º<2Ө<50°. The X-ray diffractogram, plotted between intensity of diffracted light v/s angle of scattering (2θ value) is shown in fig 4.The powder X-ray diffraction spectra of Piroxicam, prepared ... See full document
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Formulation and In Vitro Evaluation of solid dispersions of BCS Class II Drug Febuxostat by employing L-HPC
... and solid dispersions are shown in fig 9 in selected ...the solid dispersion, drug particles were entrapped in the carrier matrix and the crystalline appearance of the drug was reduced and became ... See full document
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Formulation and in vitro evaluation of sustained release dosage form with taste masking of metformin hydrochloride
... B-6 formulation shows precise sustained release of metfomin hydrochloride and follows first order kinetics with correlation coeffi cient of ...that, formulation B-6 was selected as best ... See full document
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Studies on formulation and in vitro evaluation of Glimepiride floating tablets
... The corresponding plot log cumulative percentage of drug release Vs time for Korsmeyer-Peppas indicated good linearity (r 2 = 0.986). The release exponent n was within the range of 0.490 – 0.816, which appears to ... See full document
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FORMULATION AND EVALUATION OF LIQUISOLID COMPACT OF CANDESARTAN WITH β CYCLODEXTRIN
... Spectrum was measured over a frequency range of 4000-400 cm -1 . The peaks obtained in the spectra were then compared with the corresponding functional groups in the structure of Candesartan 10 . Differential Scanning ... See full document
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