Dosage forms
EVALUATION OF IN VITRO STABILITY STUDIES ON NUTRACEUTICALS IN ORAL SOLID DOSAGE FORMS WITH SPECIAL REFERENCE TO GLUCOSAMINE
... various forms including ...of dosage forms. In the last few years controlled release dosage forms have made significant progress in terms of clinical efficacy and patient ...
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Stability indicating RP-HPLC method development and validation of cefepime and amikacin in pure and pharmaceutical dosage forms
... Various methods have been reported for analysis of cefepime (Spectrophotometry: Rambabu, Jyothirmayee, Naga Raju, 2012; Elazazy, Shalaby, 2012; Khare et al., 2012; Sujith, Abraham, Divakar, 2010; Nanda et al., 2012; ...
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INDUSTRIAL PROCESS VALIDATION OF SOLID DOSAGE FORMS: A REVIEW
... Different dosage forms have different validation ...solid dosage forms, protocol preparation and regulatory basis for process validation with special emphasis on tablets in ...
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Development and validation of a RP–HPLC method for quantization studies of albendazole suspension dosage forms of Rombendazol
... The analysis of the content in albendazole in suspensions of Rombendazole has been carried out under the developed method recommended for validation, using the reference s[r] ...
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A validated stability-indicating RP-HPLC method for paracetamol and lornoxicam: Application to pharmaceutical dosage forms
... Lornoxicam (LR), an oxicam derivative, is an NSAID. It is used for the treatment of musculoskeletal and joint disorders such as osteoarthritis and rheuma- toid arthritis. It is also used for the treatment of other ...
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Determination of fractionated heparin in pharmaceutical dosage forms using turbidimetry.
... O método foi desenvolvido e validado para a determinação da HF em micropartículas de poli-(D,L-láctico-co-glicólico) (PLGA), para cálculo da porcentagem de fármaco encapsulado e[r] ...
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A new insight about pharmaceutical dosage forms for benzathine penicillin G
... The results of the CMC determination for sodium deoxycholate are described in Table 2 and show clearly that at high ionic strength due to sodium chloride concentration of the saline solu[r] ...
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The characteristics of novel dosage forms
... ()*.. 8 NRQWDNWX VD YRGRP WDEOHWD VH EU]R UDVSDGD L RVOREDD SHOHWH 3HOHWH VDGUçH OHNRYLWX VXSVWDQFX RNUX çHQX SROLPHUQLP RPRWD HP 3ROLPHUQL RPRWD EXEUL L RPRJXþDYD XOD]DN YRGH X XQXWUDåQ[r] ...
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Artigo03 AIFernandes Final
... solid dosage forms (powders and minitablets containing known amounts of the model drugs; Table 1) intended for pediatric use were initially produced respectively from fresh and powdered commercial ...
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Braz. J. Pharm. Sci. vol.51 número2
... USP Apparatus 3 (reciprocating cylinder) is a very versatile device for the in vitro assessment of release characteristics of solid oral dosage forms, because it enables the product to be subjected to ...
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FORMULATION AND EVALUATION OF IMMEDIATE RELEASE TABLET OF CINNARIZINE AND DIMENHYDRINATE
... Immediate release tablets are those which disintegrate rapidly and get dissolved to release the medicaments. In the case of solid dosage it should dissolve or disintegrate in the stomach within a short period. ...
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Simultaneous Estimation of Lamivudine and Stavudine by using RP-HPLC and Method Development as per ICH Guidelines
... pharmaceutical dosage forms or in human plasma by high performance liquid chromatography(5,11) spectrophotometry, titrimetry, liquid chromatography/tandem mass spectrometry and high performance thin layer ...
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Quím. Nova vol.34 número2
... The present work describes a novel stability-indicating reversed-phase ultra performance liquid chromatography method for the separation and quantiication of rosuvastatin (RSV) and its related impurities in the ...
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Rev. Bras. Enferm. vol.69 número5
... liquid dosage form at the institution or in the Brazilian pharmaceutical mar- ket and that, therefore, represented a better option for patients with enteral feeding tubes, in addition to the observation that there ...
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Braz. J. Pharm. Sci. vol.53 número3
... On the basis that the main objective of this work was to develop a drying process extract of Orthosiphon aristatus extract for later elaboration of solid dosage forms, and knowing that to dry the extract ...
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Braz. J. Pharm. Sci. vol.51 número3
... Literature survey reveals spectroscopic methods for determination of ATV as single drug or in combination with other drugs (Prajapati, Bhandari, 2011; Dey, et al., 2012). In addition, some HPLC, HPTLC and stability ...
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Quím. Nova vol.34 número2
... guar galactomannan, before and after puriication, according to their phy- sicochemical properties and corresponding tablet or capsule dissolution performance. Puriication reduced the protein level (initially > 5% to ...
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Eclet. Quím. vol.35 número3
... OFL is offi cial in BP [13], USP [14] and EP [15]. The assay procedure mentioned in these pharmacopoeias is non aqueous titration. There are many reported HPLC [16-18], UV spectropho- tometry [19] and spectrofl uorimetry ...
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Braz. J. Pharm. Sci. vol.52 número3
... drug dosage forms can lead to changes in the polymorphic and morphological behaviors of drugs, which may cause therapeutic inefectiveness, because while medicines are produced and stored, they tend to seek ...
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Simultaneous determination of candesartan and hydrochlorothiazide in human plasma by LC-MSMS
... et al., 2014) methods are available for the evaluation of CAN and HCT in bulk, pharmaceutical dosage forms and in biological samples individually or in combination with other drugs. To our knowledge, no ...
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