mail
editor@ajptr.com
whatsapp
9409046853
logo

American Journal of PharmTech Research

📢 Latest Update: New special issue call for papers on "Emerging Technologies in Research" - Submit by March 31, 2025

📢 Latest Update: New special issue call for papers on "Emerging Technologies in Research" - Submit by March 31, 2025

December 2024 Issue 6

Volume 14, Issue 6 - $2024

Volume 14 Issue 6 Cover

Issue Details:

Volume 14 Issue 6
Published:Invalid Date

Editorial: December 2024 Issue 6

Welcome to the 2024 issue of American Journal of PharmTech Research. This issue showcases the remarkable breadth and depth of contemporary research across multiple disciplines. From cutting-edge applications of machine learning in climate science to the revolutionary potential of quantum computing in drug discovery, our featured articles demonstrate the power of interdisciplinary collaboration in addressing global challenges.

We are particularly excited to present research that bridges traditional academic boundaries, reflecting our journal's commitment to fostering innovation through cross-disciplinary dialogue. The integration of artificial intelligence with environmental science, the application of blockchain technology to supply chain management, and the convergence of urban planning with smart city technologies exemplify the transformative potential of collaborative research.

As we continue to navigate an era of rapid technological advancement and global challenges, the research presented in this issue offers both insights and solutions that will shape our future. We thank our authors, reviewers, and editorial board members for their continued dedication to advancing knowledge and promoting scientific excellence.

Dr Hemangi J Patel
Editor-in-Chief
American Journal of PharmTech Research

Articles in This Issue

Showing 9 of 9 articles
Research PaperID: AJPTR146001

A Comprehensive Review On Ophthalmic In Situ Gelling System

Anirban Mandal, Arindam Dutta, Anandamoy Rudra

The eye is one of the most delicate organs in our body. The eye is a complex organ characterized by its low permeability, short precorneal residence time, and small area for absorption, which pose significant barriers to drug delivery. Typically, less than 10% of a drug administered penetrates the eye. Traditional ocular delivery systems are also constrained, with significant drug loss due to tears and blinking, leading to blurred vision and untimed release events without sustained action, resulting in suboptimal outcomes in ocular therapy. To overcome such challenges, in situ ophthalmic gels have been developed. These gels' ability to transition from a liquid to a gel state allows for sustained drug release at the target site. In situ gel systems are in solution form before administration and then convert to a gel under physiological conditions (pH, temperature, or ionic concentration). This review discusses the anatomy and physiology of the eye, the challenges of ocular drug delivery, types of in situ gelling systems, mechanisms of gel formation, types of smart polymers, and methods for evaluating polymeric in situ gels.   

Ocular drug deliveryin situ gelsol-gel transitionsmart polymerssustained release.
343,198 views
102,995 downloads

Contributors:

 Anirban Mandal
,
 Arindam Dutta
,
 Anandamoy Rudra
Research PaperID: AJPTR146002

Development and validation of method for simultaneous estimation of Triple Drug Combination Employed for Type II Diabetes Mellitus and its validation using ICH Q2R1

Mounika. B, Kommineni .Vinutha, Rayeesa Seema, Sridevi P

This study reports the method development and validation for anti-diabetic drugs by UPLC.  A new, simple, rapid, selective, precise and accurate ultra performance liquid chromatography assay has been developed for simultaneous estimation of Remogliflozin, Vildagliptin and Metformin. The separation was achieved by using ODS 3V column with dimensions 5 µm, 4.6 mm x 250 mm. The pH of mobile phase was adjusted to 4.5 with acetonitrile. The flow rate was 0.4 mL/min, and the separated drugs were detected using UPLC detector at the wavelength of 260 nm. The method was validated as per ICH guidelines. The proposed method was found to be accurate, reproducible, and consistent. It was successfully applied for the analysis of these drugs in marketed formulations and could be effectively used for the routine analysis of formulations.

RemogliflozinVildagliptinMetforminICH guidelines
343,057 views
103,050 downloads

Contributors:

 Mounika. B
,
 Kommineni .Vinutha
,
 Rayeesa Seema
,
 Sridevi P
Research PaperID: AJPTR146003

Analytical Method Development and Validation for The Simultaneous Estimation Of Mirabegron and Solifenacin In Bulk and Pharmaceutical Dosage Form by RP-HPLC

K. Keerthana, K.Vinutha, P. Sridevi

A rapid stability-indicating RP-HPLC was developed and validated for the estimation of Mirabegron and Solifenacin combination in bulk and tablet dosage form using Thermo C18 column (250 x 4.6 mm, 5m) as a stationary phase and a mixture solution of 0.1 percent Diazanium sulphate buffer: Acetonitrile (60:40 v/v) as the mobile phase at a flow rate of 1 ml/min. A photodiode array detector was used for detection at 246 nm. The linearity, sensitivity, selectivity, robustness, specificity, precision, and accuracy were all determined. The peak area response-concentration curve was rectilinear over the concentration ranges of 25-75 g/ml (Mirabegron) and 2.5-7.5 g/ml (Solifenacin), with quantitation limits of 0.793 g/ml (Mirabegron) and 0.307 g/ml (Solifenacin). The proposed method was validated for the simultaneous determination of mifepristone and misoprostol in combined tablet dosage form. In comparison to previously reported RP-HPLC methods, the performance of the proposed method was found to be rapid and cost-effective. The developed and validated stability-indicating RP-HPLC method was suitable for quality control and drug analysis.

RP-HPLCstability-indicatingtablet dosage form.
343,415 views
102,964 downloads

Contributors:

 K. Keerthana
,
 K.Vinutha
,
 P. Sridevi
Research PaperID: AJPTR146004

A Review On Trigonella Foenum-Graceum Linn (Fenugreek)

Prasad S. Dhamane, Prashant S. Malpure, Gokul S. Talele, Rahul N. Chaudhari

The goal of the current work is to use the wet granulation technology to make medication tablets using fenugreek extract. Additionally, research was done on the impact of sodium starch glycolate, a super disintegrant, on drug release and disintegration. Mucilage found in fenugreek extract slows down the disintegration of tablets, resulting in a slower release of the medication. Therefore, sodium starch glycolate was employed as a super disintegrant to enhance disintegration and, consequently, in vitro drug release. Wet granulation was used to make tablet formulations both with and without sodium starch glycolate. It was done to evaluate the granules' flow characteristics and characterize the physicochemical makeup of tablet formulations. The fundamental cause of fenugreek's antidiabetic effect is the alkaloid trigonelline, which is present in large amounts. For the treatment of diabetes, this study concludes that fenugreek seed extracts in tablet form with super disintegrants will be more desirable, useful, and therapeutically more effective than combining the plant components directly for a quicker commencement of action.

Tabletsodium starch glycolatefenugreek.
343,446 views
103,009 downloads

Contributors:

 Prasad S. Dhamane
,
 Prashant S. Malpure
,
 Gokul S. Talele
,
 Rahul N. Chaudhari
Research PaperID: AJPTR146005

A Bibliographic Analyzation on Positive and Negative Impact of Paleolithic Diet

S. Sabishruthi, S. Shyamala

Paleolithic diet also known as stone-age diet, is based on those food items that were available during the Paleolithic period, which dated from 2.5 million years ago to 10,000 B.C. This diet includes food items such as meat, fish, fruits, vegetables along with a very small number of cereals, roots, eggs, nuts, and excludes items like dairy products, grains, sugar, legumes, processed or refined oils, salt, coffee or tea, and alcohol. On one hand, the Paleolithic diet is beneficial in the case of chronic conditions like type 2 DM, cardiovascular diseases, obesity, and other such conditions. On the other hand, adherence to the Paleolithic diet leads to a few adverse effects like calcium deficiency, iodine, vitamin D, and more due to exclusion criteria of some food. Furthermore, evidence of clinical trials on a large population are needed as several trials conducted on a small sample will only lead to poor results resulting in lack of evidence. On a separate note, alternative diets are also opted for compensate the lack of elements to avoid any further medical consequences. Upcoming studies should throw light on clinically analyzing the health quality of excluding certain food items in the context of Paleolithic nutrition.

Paleolithic DietBenefitsDrawbacksClinical trialschronic conditionsAlternative diets.
343,576 views
103,140 downloads

Contributors:

 S. Sabishruthi
,
 S. Shyamala
Research PaperID: AJPTR146006

21- CFR: An Important Concept Of Pharma Industry

Gaurav Kale, A. M. Bhagwat, Manish Pujari, Resham Ingawale

21 CFR is the code of federal Regulation. It is the regulation which gives by the USA/America for the pharma Industries. It is started in 1935 by the America’s 32nd President (Franklil. D. Roosevlt). It is very useful for pharma Industries in future for the Manufacturing processing packaging or holding of drug and finish pharmaceutical’s. It is the regulation for the food and drugs. This paper explores Title 21 of the Code of Federal Regulations (21 CFR), highlighting its essential role in regulating various aspects of the pharmaceutical industry in the United States. It emphasizes 21 CFR's impact on ensuring the safety, efficacy, and quality of pharmaceuticals and biologics. The paper also examines its relevance in modern regulatory practices and its global influence on regulatory compliance and good manufacturing practices (GMP).It will most useful guidelines for new Pharmacists. It is the future of the pharma Industries. Which is trying to get approval from USFDA?

21 CFRManufacturingProcessingPackagingUSFDA
343,765 views
103,179 downloads

Contributors:

 Gaurav Kale
,
 A. M. Bhagwat
,
 Manish Pujari
,
 Resham Ingawale
Research PaperID: AJPTR146007

Analytical method development and validation of Niraparib and Abiraterone using RP-HPLC method by using QbD method

Mounica B, Vinutha Kommineni, Sreedevi P

A robust RP-HPLC technique was set up for the estimation of Abiraterone & Niraparib. SST parameters, including resolution, theoretical plates, & tailing factor, were within acceptable boundaries, ensuring the technique's reliability. technique verification followed ICH rules, demonstrating high assay accuracy with recoveries within 98-102%. The linearity scale was 10-50 µg per ml for Abiraterone & 2-10 µg per ml for Niraparib, with R2 of 0.999. Precision, ID precision, & robustness tests confirmed the technique's consistency across different conditions. LOD & LOQ were established, showcasing the technique's sensitivity. This verified RP-HPLC technique is suitable for regular analysis of Abiraterone & Niraparib in l formulations.

NiraparibAbirateroneQbDRP HPLC. 
343,718 views
103,200 downloads

Contributors:

 Mounica B
,
 Vinutha Kommineni
,
 Sreedevi P
Research PaperID: AJPTR146008

Reserve Samples: An Important Concept of Pharma Industry

Manish Pujari, A. M. Bhagwat, Gaurav Kale, Omkar Dadas

Reserve samples in the pharmaceutical industry are vital for quality assurance and regulatory compliance. Retained from each production batch, these samples ensure product quality, safety, and efficacy throughout their shelf life. They play a crucial role in investigating complaints, verifying product consistency, addressing regulatory inspections, and supporting stability studies. Regulatory bodies like the FDA, EMA, and WHO require strict guidelines for their handling, storage, and retention. Reserve samples must align with the product’s labeled storage conditions and be kept for at least one year beyond the expiration date or two years after the last distribution, whichever is longer. Sufficient quantities must also be maintained to allow at least two full quality analyses. Managing reserve samples involves challenges such as storage space limitations, environmental control costs, risk of degradation, and the need for precise documentation. However, technological advancements like automated inventory systems, IoT-based monitoring, and digital record-keeping have improved efficiency and reliability. These innovations reduce risks of non-compliance and enhance traceability. This review highlights the purpose, regulatory requirements, best practices, and challenges associated with reserve samples, as well as recent technological advancements. Reserve samples are integral to pharmaceutical operations, helping companies maintain product quality standards, consumer trust, and regulatory compliance. Continuous improvement in reserve sample management is essential to meet the evolving demands of the pharmaceutical industry.

Reserve SamplesPharmaceutical QualityRegulatory ComplianceStability StudiesSample Management
344,084 views
103,231 downloads

Contributors:

 Manish Pujari
,
 A. M. Bhagwat
,
 Gaurav Kale
,
 Omkar Dadas
Research PaperID: AJPTR146009

Formulation Development of Ritonavir loaded solid lipid Nanoparticles for Targeted Drug Delivery

Swapna Velivela, D.Varun, Veena Gadicherla, D.Naga Latha

Solid lipid nanoparticles (SLNs) have emerged as a remarkable nano-colloidal system for drug delivery. This research work aims at developing and optimizing the Ritonavir loaded solid lipid nanoparticles for targeted drug delivery by solvent emulsification-evaporation method. The produced solid lipoid Ritonavir nanoparticles were characterized for various physicochemical in terms of size, surface charge, % entrapment efficiency (EE) and in-vitro drug release studies. The entrapment efficiency (%) range of solid lipid nanoparticles (SLNs) is between 16.23% to 54.23% with polydispersity index (PDI) of 0.2. The mean size of particles was found between 189.6 to 271.4 nm. This indicates particles are in uniform distribution. The zeta potential was found in the range of -36.54 to -41.57 mV for prepared solid lipid nanoparticles. The most EE% was about 54.23% achieved in the presence of Polysorbate 20. It was found that addition of Polysorbate 20 in optimized concentration in the process led to increased entrapment efficiency and particle size when compared with Span 20.  In this study, we showed the SLNs have more encapsulating Ritonavir with optimized drug release.

Ritonavirsolid lipid nanoparticles (SLNs) entrapment efficiencypolydispersity index (PDI)
344,277 views
103,258 downloads

Contributors:

 Swapna Velivela
,
 D.Varun
,
 Veena Gadicherla
,
 D.Naga Latha
Whatsapp