Pharmaceutical Sciences

All Items

• DEVELOPMENT AND VALIDATION OF HPTLC METHOD FOR THE ESTIMATION OF ESCITALOPRAM OXALATE IN BULK AND PHARMACEUTICAL DOSAGE FORM

  A.SUNEETHA, P.MUTHUPRASANNA

  504-510

• DEVELOPMENT AND VALIDATION OF LC-MS/MS METHOD FOR THE ESTIMATION OF ZALTOPROFEN ENANTIOMERS IN PHARMACEUTICAL FORMULATION

  B. GOWRAMMA, S. N. MEYYANATHAN

  883-889

• DEVELOPMENT AND VALIDATION OF NEW ANALYTICAL METHOD FOR PACLITAXEL IN BULK AND PHARMACEUTICAL DOSAGE FORM BY REVERSE PHASE HPLC (RP-HPLC)

  SREERAMAMURTHY PYLA, K.SRINIVAS, JOGENDRAKUMAR YVV, JAGADEESH PANDA

  534-540

• DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR SIMULTANEOUS ESTIMATION OF GLICLAZIDE AND SITAGLIPTIN PHOSPHATE MONOHYDRATE IN BULK AND TABLET DOSAGE FORM

  C. RUBINA REICHAL, M. GOPAL RAO

  361-369

• Development And Validation Of Rp-Hplc Method For Simultaneous Estimation Of Rosuvastatin Calcium And Aspirin In Capsule Dosage Form

  CHIRAGSINH SOLANKI, NISHITKUMAR PATEL

  577-585

• Development and validation of RP-HPLC method for simultaneous estimation of teneliglipt in hydro bromide hydrate and glimepiride in bulk and tablet dosage form

  I.PONNILAVARASAN, N.TAMILSELVI, N.ABINAYA, R.GAYATHRI

  18-25

• Development And Validation Of RP-HPLC Method For The Estimation Of Strontium Ranelate In Sachet

  K.MYTHILI, S.GAYATRI, KOYA RAVI TEJA, K.CHITRA, C.UMA MAHESWARA REDDY

  258-263

• DEVELOPMENT AND VALIDATION OF RP-HPLC PRE-COLUMN DERIVATISATION FOR THE TRACE LEVEL DETERMINATION OF TERTBUTYLAMINE IN TIGECYCLINE DRUG SUBSTANCE

  R.SRIKANTH, D.RAGHUNADHA REDDY, C.S.VENKATESAN

  522-531

• Development and validation of stability indicating reverse Phase high performance liquid chromatography method with Photodiode array detection for the simultaneous estimation of hypoglycemic agents, Dapagliflozin and Metformin

  K. LAKSHMI PRAMEELA, P. RAMA KRISHNA VENI, P. V.V. SATYANARAYANA, B. HARI BABU

  328-336

• DEVELOPMENT AND VALIDATION OF STABILITY INDICATING REVERSE PHASE LIQUID CHROMATOGRAPHIC METHOD FOR THE ASSAY OF AZELNIDIPINE IN BULK AND PHARMACEUTICAL FORMULATIONS

  RAJAN V RELE., SWAPNIL A. SAWANT

  376-380

• DEVELOPMENT AND VALIDATION OF STABILITY INDICATING RP-HPLC METHOD FOR SIMULTANEOUS ESTIMATION OF LEVOSULPIRIDE

  NANDAKISHORE AGARWAL, B.JAGADEESH

  718-726

• Development And Validation Of Stability Indicating Uv Spectrophotometric Method For The Estimation Of Atomoxetine Hydrochloride In Bulk And Tablet Dosage Form

  PARAG PATHADE, AMOL PAWAR, ABHIJIT GAIKWAD, ASHWINI PANHALKAR

  596-602

• Development of a simple, rapid and specific RP-HPLC method for the estimation of pyridoxine hydrochloride and doxylamine succinate in bulk and combined pharmaceutical dosage forms

  AMAR KUMAR KASTURI, KANAKA RAJU MEDICHERLA, N. BALAKRISHNAN

  21-28

• DEVELOPMENT OF A UPLC ASSAY METHOD OF DANAZOL USING QbD APPROACH

  MRUNALINI KULKARNI, VIKAS NAWATHYE

  227-235

• DEVELOPMENT OF A VISIBLE SPECTROPHOTOMETRIC METHOD FOR THE QUANTITATIVE DETERMINATION OF METANIL YELLOW IN DIFFERENT FOOD SAMPLES.

  PARTHA PRATIM NATH, KAUSHIK SARKAR, PANCHALI TARAFDER, GOUTAM PAUL

  685-692

• DEVELOPMENT OF ANALYTICAL METHOD FOR DETERMINATION OF LISINOPRIL TABLETS USING RP-HPLC METHOD

  V.MASLARSKA, J. TENCHEVA

  163-167

• DEVELOPMENT OF CONTROLLED RELEASE ANTIULCER TABLETS USING EXTRUSION- SPHERONIZATION METHOD AND STUDY OF EFFECT OF HYDROPHILIC POLYMERS ON RELEASE RATE AND IN VITRO EVALUATION

  S. P. PHADATARE, K. K. SINGH

  367-381

• DEVELOPMENT OF IN VITRO RELEASE TEST FOR CAPSAICIN TOPICAL GEL FORMULATIONS BY USING FRANZ DIFFUSION CELL

  PRAKASH B. MODI

  285-293

• Development of Inorganic Carrier Based Bioformulation of Sebacina Vermifera and Its Evaluation on Trigonella Foenumgraecum (Funded work)

  Kamal Jeet, Ashish Baldi

  69-82

• Development of new validated spectrophotometric method for the estimation of sulphamethoxazole & its application of protein binding studies

  K V HIMAVANI, M. SUDHEER, G. NARESH, A. PADMA, P. RAMALINGAM

  565-570

• Development Of New Visible Spectrophotometric Methods For The Determination Of Entecavir In Pharmaceutical Dosage Forms

  M. RAJESWARI, P. SUBRAHMANYAM, G. DEVALA RAO, G. SUDHAKAR SAI BABU

  91-94

• DEVELOPMENT OF SOLID SELF EMULSIFYING DRUG DELIVERY SYSTEMS CONTAINING EFAVIRENZ: IN VITRO AND IN VIVO EVALUATION

  V. KIRAN KUMAR, M. ARUNA DEVI, D.V.R.N.BHIKSHAPATHI

  869-882

• DEVELOPMENT OF SOME NEW AND SENSITIVE ANALYTICAL METHOD FOR THE ESTIMATION AND VALIDATION OF LEVOFLOXACIN BY REVERSE PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY (RP-HPLC)

  YEDLA NAGARAJ

  102-120

• DEVELOPMENT OF STABILITY INDICATING METHOD FOR VALIDATION OF LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE DRUGS IN SOLID DOSAGE FORM BY RP-HPLC

  SHAIKH ANIS

  621-638

• Development of Stability Indicating UV-Method for The Determination of Artesunate in Bulk and Pharmaceutical Dosage Form

  Gangu Sreelatha, J.S Swatantra, E. Ratna Sri, Ch. Samatha, G. BhagyaLaxmi

  57-63