e-ISSN: 2320-0812 p-ISSN: 2347-2340
Welcome to the Journal
We are delighted to invite Eminent Scientists, Academicians and Researchers to submit their original research articles for publication Research & Reviews: Journal of Pharmaceutical Analysis (e-ISSN: 2320-0812, p-ISSN: 2347-2340) an International journal publishing quarterly (Electronic and Print version) on the aspect of Pharmaceutical Analysis for an effective scientific reading and public view with an aim to reach the world wide researchers.
The manuscript would be considered under the specific branch of Pharmaceutical Analysis.
  • Analysis of Traditional Indian System of Medicine (AYUSH)
  • Pharmaceutical Analysis of Complex System
  • Quality Control and Methods of Biotech Drug
  • Quantitative and Qualitative Analysis In The Drug Screening Process
  • Tracer Analysis in Molecular Pharmacology
  • Quantitative Analysis in Biopharmaceutics
  • Biological and Radio-immuno Assays
  • Analysis of Crude Drugs
  • Thermo-Analytical Methods of Analysis
  • Sterility Testing Methods
  • Pharmaceutical Cosmetic Analysis
  • Validation: Method, Cleaning And Personal Validations

Submit manuscript at http://rroij.com/editorialtracking/pharmaceutical-analysis/SubmitManuscript.php or send as an e-mail attachment to the Editorial Office at  pharmanal@rroij.org

Recently published articles
» Is Chemo-Metrics Showing the Pathway for Unsolved Questions in Chemical / Drug Analysis?.

Ritika, Navdeep K Gill, Ravindra K Rawal, and GS Sarma

» Development and Validation of RP-HPLC Method: An Overview.

M Sangeetha, C Rubina Reichal, VN Indulatha, and N Thirumoorthy

» Chemo-Metric Evaluation of Levocetrizine Dihydrochloride, Paracetamol, Ambroxol Hydrochloride and Phenylephrine Hydrochloride in Pharmaceutical Dosage Forms.

Ritika, Madhur Arora, GS Sarma, and Ravindra K Rawal

» UV - Spectrophotometric Method Development and Validation for Determination of Raloxifene in Pharmaceutical Dosage Form.

Nagaraju PT, K Venu Gopal, Murali Krishna NV, Bhargavi V, and Srinivasulu N

» Isolation, Identification and Characterization of Unknown Impurity in Fermentation Based Active Pharmaceutical Ingredient Lovastatin.

Chandrakant Belwal, Divyesh Patel, Kamlesh Chauhan, Yogendrasinh Parmar, Ajay Singh Rawat, and Anand Vardhan

» Review on Analytical Method Development and Validation.

Review on Analytical Method Development and Validation.

» Differential Scanning Calorimetry: A Review.

Kodre KV, Attarde SR, Yendhe PR, Patil RY, and Barge VU

» UV-Spetrophotometric Method Development and Validation for Determination of Linezolid in Pharmaceutical Dosage Form.

Nagaraju PT, Sreenivasa Rao M, Ravi Kumar C, Mabhasha D, K Venu Gopal, and Murali Krishna NV

» Development and Validation of Spectroscopic Method for Simultaneous Estimation of Allopurinol and α-Lipoic Acid in Combination Tablet.

Darshan J Patel, Vineet C Jain, and Hasumati A Raj

» First Derivative Spectroscopic Method for Simultaneous Estimation of Edaravone and Citicoline Sodium in Synthetic Mixture.

Bhumi K Patel, Hasumati A Raj, and Vineet C Jain

» Validated HPTLC Method for Simultaneous Estimation of Sitagliptin and Metformin Hydrochloride in Bulk Drug and Formulation.

Snehal V Warghade, Neha N Devlekar, Ravindra Y Patil, and Vijaya U Barge

» Analytical Methodologies for the Determination of Hydralazine: A Review.

Shah Kruti V, Chauhan SP, and Suhagia BN

» Analytical Methodologies for the Determination of Sirolimus: A Review.

Shah Kruti V, Chauhan SP, and Suhagia BN

» Development and Validation of Rasagiline Tartrate in Tablets by using Liquid Chromatography.

K Vanitha Prakash, Ravi Pratap Pulla and Y Kranthi Kumar

» Validated Spectrophotometric Methods for Estimation of Telmisartan and Hydrochlorothiazide in Combined Tablet Dosage Form.

Chinmaya C Behera, Vishal Joshi, Sujit Pillai, and Gopkumar P

» Dual Wavelength Spectrophotometric Method for Estimation of Cilnidipine and Telmisartan in Their Combined Dosage Form.

Shahin Vahora, Falgun Mehta, Usmangani Chhalotiya, and Dimal Shah

» Ultraviolet Spectrophotometric Determination of Trifluoperazine. HCl in Pharmaceutical Preparations and Environmental Wastewater Samples: Application to Content Uniformity Testing.

Nief Rahman Ahmed

» Liquid Chromatographic Estimation of Epalrestat and Methylcobalamin in Pharmaceutical Formulation.

Krima R Patel, Dimal A Shah, Falgun A Mehta, Usmangani K.Chhalotiya, Kashyap K Bhatt

» Pharmaceutical Applications of Insilico methods: A Review.

AR Mullaicharam, and Nirmala Amaresh

» Development and Validation of Reversed Phase High Performance Liquid Chromatography Method for Determination of Tapentadol in Pharmaceutical Formulation.

B Mohammed Ishaq, K Vanitha Prakash, and G Krishna Mohan

» Simultaneous Spectrophotometric Estimation of Albendazole and Ivermectin in Pharmaceutical Formulation.

Rajiv Kumar Chomwal, and Anju Goyal

» Physical and Chemical Characteristics of Shea nut Fat Extracts from Selected Areas of Kebbi State, Nigeria.

AA Warra, and AJ Ahmad

» Development and Validation of a Stability Indicating RP-HPLC Method for the Determination of Valganciclovir Hydrochloride (RS).

Krishna Veni N, Gowramma B, Madhuri L, Gouthami B, Sindhur Nag N and Meyyanathan SN

» A Validated Stability Indicating Reverse Phase Liquid Chromatography Method for Metformin HCL and its Impurities in Bulk and Pharmaceutical Dosage Form.

T Sudha, Vamsi Krishna, and VR RaviKumar

» ICH Guidelines in Practice: Development and Validation of HPTLC Method for Simultaneous Estimation of Ketorolac Tromethamine and Ofloxacin in Ophthalmic Formulation.

Vrushali Tambe, Manaswi Patil, Ujjwala Kandekar, and Shrivastava SK

» Critical Factor That Governs a Successful TLC/ HPTLC Analysis of Herbal Medicinal Products (HMPS).

Rahul Kasar, Ashish Gogia, Kartik Shah, Vetriselvan and Chinmay Anand

» Development and Validation of UV/ Visible Spectrophotometric Method for the Estimation of Oxcarbazepine in Bulk and Pharmaceutical Formulations.

Arti Mohan, and SK Ghosh

» Formulation and Evaluation of Floating Nateglinide Tablets Using Factorial Design.

Om Prakash, S Saraf, M Rahman, Neeraj Agnihotri, and Vinay Pathak

» Liquid Chromatographic Method Development for the Estimation of Cefpodoxime Proxetil and Clavulanic Acid in Combined Dosage Form.

Dimal A Shah, Piyush A Chaudhary, Usmangani K Chhalotiya, Sunil L Baldania and Kashyap K Bhatt

» To Study the Biochemical Analysis of Kidney Stone by Using FTIR Spectroscopy in the Patients with Renal Calculosis.

Pawan Kumar and Sanjita Das

» RP-HPLC Method Development and Validation for the Determination of Bupropion Hydrochloride in a Solid Dosage Form.

Lovekesh Mehta, and Jitender Singh

» Method Development and Validation for Glucosamine and Chondroitin Sulphate in Soflet Form by RP-HPLC.

Parthiban Nagarajan, Sathis Kumar Dinakaran, Somsubhra Ghosh, Harani Avasarala, Maheswaran Nallayya, and David Banji

» Development and Method Validation of Baclofen by RP-HPLC in Bulk Drug and Pharmaceutical Formulation.

Kamaldeep Singh, Gurvinder Pal Singh, and Sandeep Kumar Sharma

» Development and Validation of RP-HPLC Method for Analysis of Novel Self-emulsifying Paclitaxel Formulation.

Javed Ahmad, Kanchan Kohli, Showkat R Mir, and Saima Amin

» Synthesis, Spectroscopic Characterization and Antibacterial Properties of some Metal (II) Complexes of 2-(6-methoxybenzothiazol-2- ylimino)methyl)-4-nitrophenol.

Aderoju A Osowole, Anthony C Ekennia, and Benedict O Achugbu

» Synthesis, Spectra and Biological Studies on some Metal (II) Complexes of 3-(6-methoxypyridin-3-ylimino)methyl)-6-methyl-2H-chromen-4-ol.

Aderoju A Osowole and Godwin H Etuk

» Development and Validation of a RP-HPLC Method for Simultaneous Estimation of Diacerein and Aceclofenac in Pharmaceutical Dosage Form

Narendra Nyola, Govinda Samy Jeyabalan, N Kalra, Gazala Parveen, and Suresh Choudhary

» Spectrophotometric Method for Estimation of Tenofovir Disoproxil Fumarate in Tablets

T Shela Rani, K Sujatha, K Chitra, Don Mathew Jacob, Ramya Yandapalli, D Manasa, and B Sushma

» Spectrophotometric Method Development and Validation of Valacyclovir Hydrochloride in Bulk and Pharmaceutical Dosage Form

VMK Gowtam Potnuru, Krishna Reddy Y, Arjun CH, Prasanthi P, Ramya Krishna M, and Chandra Sekhar E

» Analytical Method Development and Validation of Sitagliptine Phosphate Monohydrate in Pure and Tablet Dosage Form by UV-Vis Spectroscopy

G Jeyabalan and Narendra Nyola