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Pharmaceutical and Drugs

A cross sectional study of the availability and pharmacist’s knowledge of nano pharmaceutical drugs in Palestinian hospitals

A cross sectional study of the availability and pharmacist’s knowledge of nano pharmaceutical drugs in Palestinian hospitals

... 100 drugs ap- proved by the FDA as nano-pharmaceutical drugs avail- able in different dosage forms and for variety applications ...nano-pharmaceutical drugs in the field of cancer ...

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RP-HPLC Analytical Method Development and Validation for Simultaneous Estimation of two Drugs Nitazoxanide, Ofloxacin and its Pharmaceutical Dosage Forms

RP-HPLC Analytical Method Development and Validation for Simultaneous Estimation of two Drugs Nitazoxanide, Ofloxacin and its Pharmaceutical Dosage Forms

... two drugs Nitazoxanide and Ofloxacin from bulk drug mix and pharmaceutical dosage ...Both drugs were properly resolved having run time of ...available pharmaceutical dosage form, yielding very ...

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SIMULTANEOUS ANALYSIS OF RPHPLC METHOD DEVELOPMENT AND VALIDATION OF TERBINAFINE AND BEZAFIBRATE DRUGS IN PHARMACEUTICAL DOSAGE FORM

SIMULTANEOUS ANALYSIS OF RPHPLC METHOD DEVELOPMENT AND VALIDATION OF TERBINAFINE AND BEZAFIBRATE DRUGS IN PHARMACEUTICAL DOSAGE FORM

... with a diet and an exercise program to treat high cholesterol levels. This proposed method is simple and accurate for the analysis of above drugs in pharmaceutical dosage form. The structures of above ...

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Pharmaceutical Suply Chain Management In Supporting Drugs Avaibility In The Jkn Era In Indonesia

Pharmaceutical Suply Chain Management In Supporting Drugs Avaibility In The Jkn Era In Indonesia

... the pharmaceutical market for companies producing both generic and branded drugs, which will drive down ...the pharmaceutical industry need to be reviewed. The higher volume of drugs sales is ...

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Blockchain Technology in Pharmaceutical Industry to Prevent Counterfeit Drugs

Blockchain Technology in Pharmaceutical Industry to Prevent Counterfeit Drugs

... of pharmaceutical industry is outdated, and doesn’t provide visibility and control for manufacturers and regulatory authority over drugs distribution and it cannot withstand the 21 st century cyber-security ...

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Conversion of renewable feedstocks into polymer precursors and pharmaceutical drugs

Conversion of renewable feedstocks into polymer precursors and pharmaceutical drugs

... Chapter 4 Synthesis of pharmaceutical drugs from CNSL metathesis catalyst into the reaction containing 3-non-8-enylphenol, and after heating at 50 °C for 16 hours under 5 bar of ethylene[r] ...

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PHARMACEUTICAL STUDY FOR THE DEVELOPMENT OF NEW DRUGS THROUGH CHELATION

PHARMACEUTICAL STUDY FOR THE DEVELOPMENT OF NEW DRUGS THROUGH CHELATION

... Characterization of complexes: The composition of metal complexses was ascertained by estimating the metal, carbon, hydrogen and nitrogen by suitable gravimetric [7] or volumetric [8] , combustion method [9] and kjeldal ...

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 CHEMOMETRICS ASSISTED RP-HPLC METHOD DEVELOPMENT FOR THE SEPARATION OF SECOND GENERATION TYROSINE KINASE INHIBITORS IN BULK DRUGS AND PHARMACEUTICAL FORMULATIONS

 CHEMOMETRICS ASSISTED RP-HPLC METHOD DEVELOPMENT FOR THE SEPARATION OF SECOND GENERATION TYROSINE KINASE INHIBITORS IN BULK DRUGS AND PHARMACEUTICAL FORMULATIONS

... The present study describes a newly developed, optimized and validated isocratic RP-HPLC method for the separation of two tyrosine kinase inhibitors (Dasatinib-DST and Nilotinib-NLT) with Methyl paraben-MPB as internal ...

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“A Review on Imidazole Derivatives Having Appropriate Remedies for Extreme Diseases” by Renjima K.M, Resmy Menon, Divya Chacko, India.

“A Review on Imidazole Derivatives Having Appropriate Remedies for Extreme Diseases” by Renjima K.M, Resmy Menon, Divya Chacko, India.

... in pharmaceutical field which are pharmacologically and physiologically active and it is used in the treatment of various ...new drugs developments in imidazole derivatives show better effect and less ...

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PREPARATION AND CHARACTERIZATION OF CHITOSAN NANOPARTICLES OF INSULIN FOR NASAL DELIVERY

PREPARATION AND CHARACTERIZATION OF CHITOSAN NANOPARTICLES OF INSULIN FOR NASAL DELIVERY

... is the Higuchi dissolution constant. Higuchi model describes drug release as a diffusion process based in the Fick’s law, square root time dependent. This relation can be used to describe the drug dissolution from ...

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Assessment of the impact of pharmaceutical advertisements on patient’s drug consuming behaviour: A questionnaire based survey

Assessment of the impact of pharmaceutical advertisements on patient’s drug consuming behaviour: A questionnaire based survey

... prescription allopathic drugs (Schedule H and Schedule X) is not allowed. DTCA of only Ayush formulations that is Ayurvedic, Unani, Siddha and Homeopathy are allowed for public advertising to consumers as long as ...

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Development and validation of a stability-indicating reverse-phase ultra-performance liquid chromatography method for the simultaneous determination of netarsudil and latanoprost in bulk and pharmaceutical formulation

Development and validation of a stability-indicating reverse-phase ultra-performance liquid chromatography method for the simultaneous determination of netarsudil and latanoprost in bulk and pharmaceutical formulation

... active pharmaceutical ingredient of both NT and LT was stressed under various conditions such as acid, base, thermal, oxidative, and photolytic conditions to conduct forced degradation ...these drugs are ...

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Stability Indicating Method Development and Validation of Tenofovir Disoproxil Fumarate in Bulk and its Tablet Dosage Form by HPTLC.

Stability Indicating Method Development and Validation of Tenofovir Disoproxil Fumarate in Bulk and its Tablet Dosage Form by HPTLC.

... ABSTRACT - A novel stability – indicating high performance thin layer chromatography HPTLC assay method was developed and validated for quantitative determination of Tenofovir Disoproxil Fumarate in bulk drugs and ...

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... Where Qt is amount of drug released in time t and KH is release rate constants. Higuchi describes drug release as a diffusion process based in the Fick’s law, square root time dependent. This relation can be used to ...

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An Overview of Pharmaceutical Co-Crystal

An Overview of Pharmaceutical Co-Crystal

... through pharmaceutical co-crystals draw closer the fields of crystal engineering and pharmaceutical sciences 9,10 ...A pharmaceutical co-crystal is a single crystalline solid that incorporates two ...

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Plant toxins: alkaloids and their toxicities

Plant toxins: alkaloids and their toxicities

... The use of alkaloids as a drug in human history has revealed the importance of these compounds in the pharmaceutical industry. For instance, the alkaloid derived from beta-carboline group such as harmine has been ...

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SOLID DISPERSION TECHNOLOGY, A CONTEMPORARY OVERVIEW ON A WELL ESTABLISHED TECHNIQUE

SOLID DISPERSION TECHNOLOGY, A CONTEMPORARY OVERVIEW ON A WELL ESTABLISHED TECHNIQUE

... Solid dispersion technology has been considered one of the well-established techniques in formulation of poorly-soluble drugs. Like every technique, it has several advantages and disadvantages that were discussed ...

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REGISTRATION PROCESS OF GENERIC DRUGS IN USFDA

REGISTRATION PROCESS OF GENERIC DRUGS IN USFDA

... Generic drugs: A generic drug is a pharmaceutical product, usually intended to be interchangeable with a new drug (an innovator product) that is manufactured without a license from the innovator company and ...

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RECENT ADVANCES IN SEMISOLID DOSAGE FORM

RECENT ADVANCES IN SEMISOLID DOSAGE FORM

... ABSTRACT: Pharmaceutical semisolid preparations include ointments, pastes, cream, emulsions, gels, and rigid ...for drugs that are topically delivered by way of the skin, cornea, rectal tissue, nasal ...

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Strategies and current scenario of Pharamcovigilance in India

Strategies and current scenario of Pharamcovigilance in India

... new drugs are being introduced in our ...the Drugs Controller General of India has been attempted to implement a pharmacovigilance program in India along with its training ...of pharmaceutical ...

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