e-ISSN: 2320-0812 p-ISSN: 2347-2340

About 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

For manuscript submission go through the below link


or send as an e-mail attachment to the Editorial Office at pharmanal@rroij.org

Pharmaceutical Analysis

Pharmaceutical Analysis is an Analytical Method used to determination the quality and quantity of the pharmaceutical products. It also gives the information about the purity and safety of the products. Briefly it can be described as it identifies, determines, quantifies, purifies and separates the active compound from the mixture.

High-Performance Liquid Chromatography

High-Performance Liquid Chromatography is an analytical technique used to separate the compounds in a mixture, to identify each component, to quantify and purify the component. High performance liquid chromatography is an improved technique form of column chromatography. Absorption is the principle involved in this technique.

Paper chromatography

Paper chromatography is an analytical method used to separation of pigments i.e. color substances or chemicals. This can use in ink experiment for detecting primary or secondary colors. Advanced technique thin layer chromatography takes the place of this technique but still it is used.

Quality Assurance

Quality assurance is the maintenance of a desired level of quality during a service or product, particularly by means that of attention to each stage of the method of delivery or production.


Prescription is an instruction given by physician. The prescription is for pharmacists to prepare the prescribed dose of medicine for patients, and for patients to follow the instructions and use the medicine for prevent or cure of diseases.

Liquid Chromatography

Liquid Chromatography is a technique used to separation of a liquid sample into its individual parts. Based on the mobile phase and stationary phase the separation of takes place. Liquid-solid column chromatography is the common chromatography in this liquid mobile phase filters through the solid stationary phase, causing separation of compounds in that.


Polarimetry in analytic chemistry is a sensitive technique for measuring the optical activity of inorganic and organic compounds. A compound is said to be optically active if polarized light is rotated when passing through it.


Titration is a technique used to determine the concentration of unknown solution by using known solution concentration. The known solution i.e. titrant is taken in burette and the unknown solution titrate is taken in beaker. The titrant is added from a burette to titrate until desired end point (as a color change) is reached.


Gravimetry is a quantitative measurement of a pure analyte, usually involving the precipitation, filtration, drying, and weighing of the precipitate. For example analysis of solids present in a water sample. Water is filtered and the remaining solid precipitate is collected and weighed.

Bio Analysis

Bio Analysis is a type of analytical method generally takes place in biological system. They analyses the small drug particles and its metabolites content in our body. Bioanalysis used for drugs used in illegal purposes, forensic science, toxicology, anti-doping testing in sports.

Gas Chromatography

Gas Chromatography is a chromatography used in analytical chemistry for separating and analyzing chemicals which have volatile nature i.e. they can be vaporized without decomposition. GC mainly used for testing the purity or separating the different compounds in a mixture. The mobile phase is a carrier gas, usually an inert gas (helium). The stationary phase is a liquid or polymer on an inert solid etc…

Thin-Layer Chromatography

Thin-Layer Chromatography is a chromatography technique used to separate non-volatile mixtures. Thin-layer chromatography the stationary phase may be a sheet of glass, plastic, or aluminum foil, which is coated with a thin layer of adsorbent material, usually silica gel, aluminum oxide, or cellulose. It is advanced technique of paper chromatography.

Gel Permeability

The another word of Gel Permeability is size exclusive chromatography which is used to separate the compounds based on molecular sizes. Gels are used as stationary phase and mobile phase should be a good solvent. The smaller molecules which are trapped in the gels elude later and the larger molecules eludes first.

Analytical Method

An analytical method is a technique that is used for quantitative and qualitative analysis of a chemical compounds. Lots of techniques used, from simple gravimetric analysis, titrimetric to very advanced techniques like HPLC, Gas Chromatography, and UV –visible spectroscopy etc…


Chromatography is used to separate the compounds from their mixture. They contain stationary phase and a mobile phase. The mobile phase passes through the stationary phase, the components which have affinity towards mobile phase elude faster and the components affinity towards stationary phase eludes later. No two components have same affinity.


If any atom or ion travels from exited state to ground state it emits radiation called fluorescence. When an atom travels from high energy to low energy ground state because of stability (ground state is more stable than exited state) it releases some energy to come to ground state that energy is called fluorescence.


A patent is a protection form granted by government state to person or legal entity with exclusive rights for processing, designing or selling a concept or invention and excludes public from using the concept in the duration of the patent.

Chemical Analysis

Chemical Analysis deals with the information about the chemical compounds. In chemical analysis it identifies, separates and structure elucidates the atoms or group of atoms present in a molecules. The chemical analysis may be quantitatively or qualitatively done.

Medicinal Products

Medicinal Product is a substance or its combination used for treating or preventing disease in humans or in animals. It also used with a view to making a medical diagnosis, modifying physiological functions in humans or animals.

Clinical Laboratory

Medical Technology is another term for Clinical Laboratory, is that the profession that has laboratory info and services required for the diagnosing and treatment of disease to get information about the health of a patient.

Clinical Research

In this Clinical Research human subjects or groups are involved. It is a research for determines the safety and effectiveness of medications, diagnostic products and treatment protocols meant for human use. It also involves the scientific analysis of the etiology, prevention, diagnosis, treatment of diseases.

Biotechnology Product

The Biotechnology products are obtained by using of living organisms or systems to develop the medicinal products for improving the health quality. Red biotechnology is a branch involves medical processes i.e. production of new drugs from organisms, regeneration of damaged tissues or re-grows the entire organs by using stem cells.

Molecular Pharmacology

Molecular pharmacology is a branch of pharmacology which is deals with the study of pharmacology on a molecular basis. It also defines mechanisms of drug action and how drugs influence the organism by studies on intact animals, organs, cells, subcellular compartments and individual protein molecules. Example when we take antibiotic for an infection how the antibiotic will attack bacteria and how the bacteria will protect themselves by developing resistance on that drug etc… are come under this.

Quality Control Areas

Quality Control Area is a part in Pharmaceutical industry present at production area ensures the quality and purity of manufacturing pharmaceutical products. It gives the information about whether the manufacturing product meets the required needs or not.

Production Area

Production Area is one of the divisions in Pharmaceutical industry where of designing brand new drugs and manufacturing efficient product.

Recently published articles
» A Review on Chromatography with High Performance Liquid Chromatography (HPLC) and its Functions

Sneha Lakshmi R.P

» A Short Commentary on Bioanalytical Techniques

N Venkateswarlu

» A Review on Capillary Electrophoresis-Mass Spectrometry (CE-MS)

Venkateswarlu N

» ?Elvitegravir? and its Validation: A Review

Sneha Lakshmi R.P

» Floating Tablets of Glipizide using Eurayle Ferox seeds for the treatement of Diabetis Mellitus

Sasidhar R

» Evaluation of Oral Mucoadhesive Metoprolol succinate Controlled Release Tablets

Sasidhar R

» Analytical Validation Parameters

Sowjanya P*1 and Subashini D 2, Lakshmi Rekha K3

» Importance of Ultra Pressure Liquid Chromatography

Priyanka R

» Method development and Validation Parameters of UV- A Commentary

Durga aruna R

» A Short commentary on Gas Chromatography and its applications

P. Udaya Lakshmi

» Method Development and Validation Parameters of HPLC- A Mini Review

L.R.D.Bhavani*, Durga aruna R

» Effect of Inhibitors on Ethanol Production: A Mini Review

Sindhu P

» Method Development and Validation of HPLC for Detremination of Levetiracetan and Valsartan in their Formulations

L.R.D.Bhavani*, Durga aruna R

» Characterisation of Sustained Release Bilayer Tablets of Pioglitazone and Metformin

Sasidhar R

» Solid dosage forms: Tablets

Nagashree K

» 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


Follow us