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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

October 2024 Issue 5

Volume 14, Issue 5 - $2024

Volume 14 Issue 5 Cover

Issue Details:

Volume 14 Issue 5
Published:Invalid Date

Editorial: October 2024 Issue 5

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 10 of 10 articles
Research PaperID: AJPTR145001

A Quality Control Study of Different Brands of Atorvastatin Tablets

Baiju Mathews, Afiya Jaleel, Seethalekshmi S, Anaghalakshmi, Athesai Roy, Jyothish B

To be considered a quality drug, a pharmaceutical tablet must meet specific standards. Key quality criteria for any drug in dosage form include safety, potency, efficacy, stability, patient acceptability, and regulatory compliance. These quality aspects must be established during the product development stage, where physical, chemical, and biological specifications are determined to ensure the product meets quality requirements. Our study aimed to determine and compare the percentage labeled claim, quality, and physicochemical characteristics of different brands of atorvastatin tablets using official and unofficial quality control tests. Atorvastatin, an HMG- CoA reductase inhibitor (statin), is essential for preventing hypercholesterolemia and related diseases. Although cholesterol is crucial in daily bodily functions, it can contribute to atherosclerosis development. We selected five brands of atorvastatin tablets (Atorva 40mg, Aztor 40mg, Lipicure 40mg, Lipikind 40mg, Lipvas 40mg) for analysis. Each sample underwent tests for hardness, friability, weight variation, disintegration, dissolution, and assay according to Indian Pharmacopoeia (IP) standards. All brands met the IP limits for hardness (4-8 kg/m2) and also complied with the requirements for weight variation and friability. The disintegration time for all brands was within the 30-minute IP recommendation for film-coated tablets. Each brand exhibited over 85% drug release within 30 minutes, and the content ranged from 90% to 110% of the labeled claim. These findings indicate that all tested atorvastatin brands available in Kerala (Kanjirappally) meet IP quality requirements.

AtorvastatinQuality controlPharmaceutical TabletsPhysicochemical CharacteristicsHypercholesterolemiaIndian Pharmacopoeia
342,040 views
102,632 downloads

Contributors:

 Baiju Mathews
,
 Afiya Jaleel
,
 Seethalekshmi S
,
 Anaghalakshmi
,
 Athesai Roy
,
 Jyothish B
Research PaperID: AJPTR145002

A Review On 3D Printing Technologies In Pharmacy

V. Swathi, J. N. Suresh Kumar, M. Harika, SK. Nagurbi, S. Suchitra, V. Tharuni, P. Kethana Kumari

3D Printing, or additive manufacturing, revolutionized various industries by enabling production of complex geometries with minimal waste and cost. 3D printing has been integrated with digital design and manufacturing process, emphasizing it’s potential to accelerate prototyping, customize production, and enhance supply chain efficiency. The current advancements in 3D Printing technologies, including material innovations, process optimizations, and applications across diverse fields such as healthcare, aerospace, automotive industry, innovative industry and consumer goods are focused with future scope for its potential usage in manufacturing products especially in medical sector.

3D printersorgan implantationanticipatedconventional methodoperations.
342,200 views
102,672 downloads

Contributors:

 V. Swathi
,
 J. N. Suresh Kumar
,
 M. Harika
,
 SK. Nagurbi
,
 S. Suchitra
,
 V. Tharuni
,
 P. Kethana Kumari
Research PaperID: AJPTR145003

Mucoadhesive Drug Delivery System – A Novel Approach For Oral Cavity Drug Delivery

Walmik Patil, Gaurav Goyanar

The mucosal layer represents a potential site for the attachment of bio-adhesive drug delivery systems, as it lines several parts of the body such as the gastrointestinal tract, urogenital tract, vaginal tract, eyes, ears, and nose. Among these, oral transmucosal drug delivery has gained more attention compared to other mucoadhesive systems like vaginal, rectal, nasal, and ocular delivery. The buccal mucosa, in particular, is rich in vascular and lymphatic systems, which allows drugs to be absorbed directly into the systemic circulation, bypassing the first-pass metabolism in the liver and avoiding pre-systemic elimination in the gastrointestinal tract. Moreover, buccal drug delivery can be quickly discontinued in case of toxicity, making it a safer and more convenient method of drug administration. This system takes advantage of the physicochemical properties of both the drug formulation and the mucosal lining. It's important to note that the mucoadhesive properties of a dosage form are only effective on moist surfaces.

Oral transmucosalBuccal mucosa
341,852 views
102,694 downloads

Contributors:

 Walmik Patil
,
 Gaurav Goyanar
Research PaperID: AJPTR145004

Regulatory requirements on parenteral dosage forms as per CDSCO in India comparison with south Africa

Ashok Kumar P, Preethi B, Nithyashree M, Navya H C, Srujana G, Poornima CS

Parenteral products are currently widely utilized in emergency situations since they provide the highest bioavailability. Parenteral product legislation is crucial as non-sterile, non-pyrogenic products can provide a serious health risk to patients, potentially leading to death. The Central Drugs Standard Control Organization (CDSCO) in India and South African health products regulatory authority (SAHPRA) in South Africa have specified different dosage formats, and this review offers a comparative examination of those requirements. This review explores critical aspects including governing legislation, clinical trial requirements, good manufacturing practices (GMP), quality control, packaging and labelling standards, import and export regulations and recent reforms. As indicated above comparative analysis of regulation and registration process for parenteral dosage from will be valuable regulatory point of view as well as business development point. With this viewpoint industry can unify dossier application in better method, which would aid in lowering time for product to go in market.

Parenteral productsCDSCOSAHPRAGMP.
342,015 views
102,688 downloads

Contributors:

 Ashok Kumar P
,
 Preethi B
,
 Nithyashree M
,
 Navya H C
,
 Srujana G
,
 Poornima CS
Research PaperID: AJPTR145005

Formulation and Evaluation of Lornoxicam Fast dissolving tablets

Ravi Degala, Govinda Kamala, Vydani Krishnaveni, Sowjanya Vadrevu4 Arshika Farzeen

Lornoxicam, is a widely prescribed Non-steroidal anti-inflammatory drug belongs to class II under BCS classification and exhibit low and variable oral bioavailability due to its poor aqueous solubility. It needs enhancement in the dissolution rate in its formulation development.  The main objective was to formulate and evaluate Lornoxicam FDT by incorporating the Lornoxicam solid dispersion to enhance dissolution rate and solubility rate with the aid of novel polymers by adopting design of experiment CCD software technology. Nine SD formulations prepared with varying concentrations of PEG 4000, Labrasol, Soluplus, Kolliphor EL, Kolliwax GMS II, HPMC, Colloidal Silicone dioxide (Aerosil 200), and PVPK25 in three different drugs : polymer : surfactant (SLS) ratios of1:1:1,1:2:1 and 1:3:1 by solvent evaporation method and were evaluated for drug content,% practical yield and dissolution rate and solubility studies. The solubility study indicates that formulation (SD9) containing drug: Soluplus (1:3) and SLS has superior solubility of 0.68±0.10µg/ml, which is 75-fold higher than pure drug. The formulations SD9 maximum percentage yield and drug content. The optimized Lornoxicam solid dispersion (SD9) was further used to prepare FDT by direct compression method using 33 Response surface method (3variables and 3 levels of super disintegrants) by using Design of experiments of tware with super disintegrants like locust bean gum, gum karaya, plantago ovate and diluents such as mannitol, Avicel PH101 and aspartame as sweating agent and aerosol as anti adherent. Total 27 Lornoxicam FDTs formulated using natural super disintegrants locust bean gum, gum karaya, plantago ovate mucilage with varying concentrations by design of experiment tool. All the formulations evaluated for various parameters such as compatibility studies, drug content, weight variation, hardness, thickness, friability, disintegration time, in vitro drug release studies. The formulation LF24 showed highest drug release of 99.21±1.87 % at 10mins. LF24 was found to be optimized formulation which contains different concentrations of locust bean gum, gum karaya, plantago ovate mucilage the results were analysed by ANOVA and FTIR studies which shows no interaction between the ingredients. The % CDR of Lornoxicam FDT (LF24) was much higher than that of Lornoxicam marketed formulation. Thus, Lornoxicam FDTs using natural super disintegrants like locust bean gum, gum karaya, plantago ovate mucilage were suitable combinations for formulating Lornoxicam FDTs.

Lornoxicam fast dissolving tabletscentral composite design(CCD)Locust bean gumgum karayaplantago ovate mucilage super disintegrantsmannitol+2 more
342,537 views
102,734 downloads

Contributors:

 Ravi Degala
,
 Govinda Kamala
,
 Vydani Krishnaveni
,
 Sowjanya Vadrevu4 Arshika Farzeen
Research PaperID: AJPTR145006

Development and Characterization of Miglitol As Immediate Release and Metformin HCL As Sustained Release Bilayered Tablets

Yella Sirisha

The purpose of this research work was to formulate an anti-diabetic in a single dosage form i.e. Metformin HCl in sustained release layer and Miglitol in immediate release layer of the bilayer tablet. The tablets were prepared using Hydroxypropyl methylcellulose (HPMC K4M & HPMC K15M, sodium alginate and xantham gum) an as release retarding polymers in various combination and concentrations. The effect of different super disintegrants on immediate release in various concentrations was also studied. Eight formulations of immediate release layer were prepared using SSG and CCS super disintegrants with different proportions and were evaluated for different parameters. Among the eight formulations M4 containing CCS as disintegrant showed a better release of 95.50±0.15% for 30 mins was selected. Using this MT4 formulation eight formulations of sustained release layer of Metformin. HCL was prepared with HPMC k15M polymer and evaluated. Among nine formulations of bilayered tablets MM4 was showed 98.66±0.65% at the end of 8 hrs. was selected as optimized formulation.  This optimized formulation was evaluated for parameters like, thickness, hardness, friability, weight variation, drug content, in vitro   drug release and stability and results were found to be with in  USP limits.

Bilayer TabletsSSGCroscarmellose sodiumHydroxypropyl methylcelluloseMetforminMiglitol+1 more
342,264 views
102,694 downloads

Contributors:

 Yella Sirisha
Research PaperID: AJPTR145007

UPLC-MS analyses and evaluation of the antimycobacterial activity of extracts of leaves and stems of Anogeissus leiocarpus and Saba senegalensis from the north of Ivory Coast

Ambeu-Loko N’ta Christelle Mélissa, Ouattara Logopho Hyacinthe, N’guessan Patrick Audrey, Yéo Sigata, Zon Doumadé, Kablan Ahmont Landry Claude

The aim of this work was to identify the main phytocompounds and to assess the antimycobacterial activity of the aqueous and ethanolic extracts of the leaves and stems of Anogeissus leiocarpus and Saba senegalensis with a view to proving or disproving their use in the treatment of tuberculosis. Evaluation of the antimycobacterial activity showed that the aqueous extract of A. leiocarpus leaves exhibited activity against two Mycobacterium tuberculosis strains used. This activity could be justified by the presence of polyphenols and alkaloids identified by UPLC-MS analysis. Organ extracts from the two plants identified polyphenols (coumarins, flavonoids, flavonols and quercetin) and alkaloids (hordenine, caffeine and nicotine) with recognised pharmacological properties. Some plants, such as A. leiocarpus could be used to treat tuberculosis. A study of the toxicity of the aqueous extract of A. leiocarpus leaves will be carried out with a view to producing a drug for treating tuberculosis.

Anogeissus leiocarpusSaba senegalensisphytocompoundsMycobacterium tuberculosisdrug.
342,329 views
102,793 downloads

Contributors:

 Ambeu-Loko N’ta Christelle Mélissa
,
 Ouattara Logopho Hyacinthe
,
 N’guessan Patrick Audrey
,
 Yéo Sigata
,
 Zon Doumadé
,
 Kablan Ahmont Landry Claude
Research PaperID: AJPTR145008

Survey of Quality Control of Dental X-ray Machines in Private Clinics in Riyadh

Faisal Almutairi, Saud Alqahtani, Mohammed Alnafea

Implementing a quality assurance (QA) program facilitate a radio diagnostic machine in acquiring sufficient radiological information of superior quality while minimizing the radiation dose administered to the subject. Integral to this program is Quality Control (QC), which ensures quality through various measurements and procedures. The main objective of this study is to assess the compliance of private dental clinics operating dental X-ray machines in Riyadh with the QC requirements. Fifteen private dental clinics in different areas in Riyadh selected and examined in the study. QC tests performed on all different X-ray machines from different manufacturers. The QC tests were kV accuracy and reproducibility, exposure time accuracy and reproducibility, and beam quality in terms of Half-Value Layer (HVL). Of the surveyed devices, two did not pass all the criteria for QC requirements. The dental X-ray machine that did not pass i.e. failed exclusively in kV accuracy but passed all the remaining QC tests. Particularly the exposure time reproducibility and Kilovoltage Accuracy. It is essential to establish a QC program in private dental clinics operating radiation-producing machines such as dental X-ray machines as it is important to ensure their compliance with the national standards for radiation safety.

QC testsDental radiographyKilovoltage accuracyRadiation protection.
342,498 views
102,735 downloads

Contributors:

 Faisal Almutairi
,
 Saud Alqahtani
,
 Mohammed Alnafea
Research PaperID: AJPTR145009

Nanoparticals As A Novel Drug Delivery System : A Review

Poonam Ankush Jadhav, Sakshi Gadekar, Bhakti Gade

Nanotechnology is the science that deals with matter at the scale of 1 billionth of a meter and is also the study of manipulating matter at the atomic and molecular scale. Recently particulate systems like nanoparticles have been used as a physical approach to alter and improve the quality of human life. The potential use of polymeric nanoparticles as carriers for a wide range of drugs for therapeutic applications has been increased due to their versatility and wide range of properties Different types of nanoparticulate material used in electronic, magnetic pharmaceutical, cosmetics, energy, catalytic and material industries. In this review the synthesis method of nanoparticles and their applications has been discussed Keywords:  Nanoparticles, Methods of preparation evaluation, route of administration

NanoparticlesMethods of preparation evaluationroute of administration
342,894 views
102,925 downloads

Contributors:

 Poonam Ankush Jadhav
,
 Sakshi Gadekar
,
 Bhakti Gade
Research PaperID: AJPTR145010

Study of the Cutaneous Toxicity and Antifungal Activity of Senna Podocarpa, A Plant Used to Treat Cutaneous Affection

Agré Don Josette, Assemian Inès Christelle Chadon Alphonsine, KONAN Gbê Kouakou N’Dri Ange, Bolou Gbouhoury Eric-Kevin

The study aims to evaluate the cutaneous toxicity and antifungal activity of the hydroethanol extract of Senna podocarpa, a plant used in traditional medicine. This research is essential to determine both the safety of using the extract on the skin and its efficacy against various fungal infections. Following OECD Guideline 404 (2015), twelve Hyplus rabbits were treated with 200 mg/kg and 500 mg/kg doses of the extract to observe skin reactions such as erythema and oedema for 14 days. Antifungal activity was assessed using the double dilution slant tube method, followed by inoculation with Candida albicans, Aspergillus fumigatus and Trichophyton mentagrophytes. Antifungal parameters such as MIC, MFC and IC50 were determined. Senna podocarpa extract showed no dermal toxicity, with a mean irritation index (MII) of 0, indicating that it is neither irritating nor corrosive to rabbit skin. No skin lesions were observed and the fur of the rabbits regrown 24 hours after application. In addition, the extract did not affect the weight of the rabbits, with those given 500 mg/kg actually showing greater weight gain than those given 200 mg/kg. In terms of antifungal activity, the extract inhibited the growth of the fungi tested in a dose-dependent manner. The MIC and MFC were 6.25 mg/mL and 12.5 mg/mL for A. fumigatus, 25 mg/mL and 100 mg/mL for C. albicans and 100 mg/mL for T. mentagrophytes.

Senna podocarpaantifungalcutaneous toxicity.
342,983 views
102,823 downloads

Contributors:

 Agré Don Josette
,
 Assemian Inès Christelle Chadon Alphonsine
,
 KONAN Gbê Kouakou N’Dri Ange
,
 Bolou Gbouhoury Eric-Kevin
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