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Journal of Pharmaceutical Research and Integrated Medical Sciences

📢 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

JPRIMS, Vol-2, Issue-7, July-2025

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Editorial: JPRIMS, Vol-2, Issue-7, July-2025

Welcome to the issue of Journal of Pharmaceutical Research and Integrated Medical Sciences. 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. Arpan Kumar Tripathi
Editor-in-Chief
Journal of Pharmaceutical Research and Integrated Medical Sciences

Articles in This Issue

Showing 10 of 10 articles
Research PaperID: JPRIMS910105

3D PRINTING IN PERSONALIZED MEDICINE: A PHARMACEUTICS PERSPECTIVE

Srikumar Chakravarthi, Rajan Rajabalaya, Sheba R David, Mohammad Nazmul Hasan Maziz, Prarthana Kalerammana Gopalakrishna

The technology and ability of 3D printing have transformed the sphere of personalized medicine, allowing manufacturing of the customized drug delivery to address diverse needs of a specific patient with regard to physiologic, pharmacokinetically, and therapeutically oriented preferences. This review generates a pharmaceutics-oriented view of the use of novel 3D printing technologies such as the Fused Deposition Modeling (FDM), Stereolithography (SLA), and inkjet printing in the development of personalized dosage forms comprising of oral tablets, implants, microneedles, and transdermal patches. Animal model experimental preclinical research, such as that in rabbits, rats, and mice, has proven the capability of the technologies to perform zero order release and controlled release of drugs, the capability to release multiple drugs using staggered kinetics, and to provide site-specific or minimally invasive delivery. The results support the benefits of structural flexibility, programmable release profiles, and improved patient adherence, especially in the case of complex conditions and important vulnerable groups of patients (pediatric and geriatric). But there are still some impediments on the way to clinical application, such as thermal instability of labile drugs, biocompatibility issues, poor reproducibility in device operation, a lack of standard regulatory frameworks, and insufficient long-term safety documentation. The review ends with a purpose of identifying the future research and development directions that include the necessity of the use of superior biocompatible materials, inherent hybrid printing methods and scalability in production, as well as interdisciplinary cooperation to enable clinical translation and redefine the future of personalized drug treatment.

Azadirachta indicaWithania somniferaHigh-Performance Liquid Chromatography (HPLC)Thin Layer Chromatography (TLC)Phytochemical fingerprinting
6,200 views
1,891 downloads

Contributors:

 Srikumar Chakravarthi
,
 Rajan Rajabalaya
,
 Sheba R David
,
 Mohammad Nazmul Hasan Maziz
,
 Prarthana Kalerammana Gopalakrishna
Research PaperID: JPRIMS910106

Design of Liposomal Drug Delivery Systems for Enhanced Cancer Therapy

Srikumar Chakravarthi, Barani Karikalan, Dr.B.Ranjith Karthekeyan, Mohammad Nazmul Hasan Maziz, Rajan Rajabalaya

Liposomal drug delivery methods are becoming popular nanocarriers for anticancer drugs because they make the drugs more available, target them more accurately, and lower their toxicity in the body. The goal of this project was to improve cancer treatment results by designing, formulating, and testing liposomal systems that include a model chemotherapeutic drug. We used the thin-film hydration approach to make three liposomal formulations (F1, F2, and F3) and then measured their particle size, zeta potential, polydispersity index, and entrapment efficiency. Studies of drug release in vitro showed that the drugs were released over time, with F3 exhibiting the largest cumulative release (89% at 24 hours). The MTT assay showed that F3 dramatically reduced the viability of MCF-7 cells (to 12% at 50 µg/mL), making it better than both other formulations and the free medication. One-way ANOVA statistical analysis showed that there were substantial differences (p

Preclinical Studies.PolypharmacyInkjet PrintingSLAFDMDrug Delivery Systems+2 more
6,069 views
1,934 downloads

Contributors:

 Srikumar Chakravarthi
,
 Barani Karikalan
,
 Dr.B.Ranjith Karthekeyan
,
 Mohammad Nazmul Hasan Maziz
,
 Rajan Rajabalaya
Research PaperID: JPRIMS910107

Development And Evaluation of Mucoadhesive Buccal Tablets for Anti-Diabetic Drugs

Rohini Armo

The need for alternative drug delivery methods that enhance patient compliance and therapeutic efficacy has been brought to light by the rising incidence of diabetes mellitus and the drawbacks of traditional oral therapy. In order to improve bioavailability by avoiding first-pass metabolism, this study concentrated on the formulation, development, and assessment of mucoadhesive buccal tablets of metformin hydrochloride. Using the direct compression method, five formulations (F1–F5) were created with different concentrations of the mucoadhesive polymers sodium alginate, HPMC, and carbopol 934. Physical characteristics, mucoadhesive strength, swelling index, surface pH, uniformity of drug content, and in-vitro drug release over an 8-hour period were all assessed for the tablets. With the best mechanical strength, the highest mucoadhesion (30.4 g), the most sustained drug release (93.7%), and controlled swelling (68%), formulation F5 outperformed the others. Significant variations between formulations were validated by statistical analysis employing ANOVA and Tukey HSD, confirming the influence of polymer concentration on drug release kinetics. According to the study's findings, mucoadhesive buccal tablets present a viable and patient-friendly substitute for the regulated administration of medications such as metformin hydrochloride, which are used to treat diabetes.

MCF-7 cellsDrug delivery systemCytotoxicityControlled releaseNanocarriersCancer therapy+1 more
6,167 views
1,933 downloads

Contributors:

 Rohini Armo
Research PaperID: JPRIMS910108

Evaluation of Floating Drug Delivery Systems for Gastroretentive Applications

S J Shankar, Akshatha R S, Kushal N, Deepika U, Ashwini K V

Floating Drug Delivery Systems (FDDS) offer a promising approach for enhancing the gastric retention time of orally administered drugs, especially those with a narrow absorption window in the upper gastrointestinal tract. This study aimed to formulate and evaluate FDDS tablets using different concentrations of hydrophilic polymers and gas-generating agents to ensure prolonged gastric residence and sustained drug release. Four formulations were prepared by direct compression and assessed for physical properties, buoyancy behavior, swelling index, drug content uniformity, and in vitro drug release over 12 hours. Among them, Formulation F4 demonstrated optimal performance, exhibiting the shortest floating lag time (25 seconds), longest floatation (>12 hours), highest swelling index (162%), and maximum cumulative drug release (96.7%). One-way ANOVA confirmed statistically significant differences in drug release and swelling index among the formulations (p

In-Vitro Drug ReleasePolymer ConcentrationDiabetes MellitusCarbopol 934HPMCSustained Release+2 more
6,294 views
1,863 downloads

Contributors:

 S J Shankar
,
 Akshatha R S
,
 Kushal N
,
 Deepika U
,
 Ashwini K V
Research PaperID: JPRIMS910109

Formulation And Characterization of Ph-Sensitive Nanoparticles for Targeted Drug Delivery

Swetha Swetha. M

The development of targeted medication delivery systems has created new ways to improve treatment outcomes, especially with the help of nanotechnology. The goal of this work was to create and describe pH-sensitive nanoparticles that would improve drug delivery by releasing the drug more in the intestines or other physiological settings and less in the stomach. We made nanoparticles in a lab by changing the ratio of polymer to drug using Eudragit® S100, PLGA, and chitosan. Characterization showed that larger polymer concentrations made the particles bigger (145–203 nm) and gave them more negative zeta potentials, which meant they were more stable. The efficiency of drug entrapment ranged from 61% to 84%, and it got better as the amount of polymer rose. SEM analysis indicated that the particles were spherical and evenly spread out. In vitro release assays showed that the drug's release depended on pH, with the least release at pH 1.2 and the most release between pH 6.8 and 7.4. ANOVA and Tukey HSD statistical tests showed that these results were strong. In general, the work shows that pH-sensitive nanoparticles could be good carriers for targeted oral medication administration.

Polymer ConcentrationIn Vitro EvaluationHPMCSustained ReleaseSwelling IndexGastroretentive Tablets+1 more
6,614 views
1,897 downloads

Contributors:

 Swetha Swetha. M
Research PaperID: JPRIMS910110

Optimization Of Fast Dissolving Tablets Using Design of Experiments (DOE)

S J Shankar, Mrs. Akshatha R S, Mr. Kushal N, Ms. Harshitha Shetty B S, Yashashwini M

Fast-dissolving tablets (FDTs) are a new type of oral dose form that breaks down quickly in the mouth without water. They are great for kids, older adults, and people who have trouble swallowing. The goal of this study was to improve the formulation of FDTs using paracetamol as a model drug. It did this by using a 3² full factorial Design of Experiments (DoE) to look at how the concentrations of superdisintegrant and binder affected important quality factors like disintegration time, hardness, friability, and drug release. Direct compression was used to make nine formulations (F1–F9), which were then tested using standard pharmacopeial assays. Using ANOVA for statistical analysis, we found that higher quantities of superdisintegrant made the tablets break down faster and release the medicine better, while the amount of binder affected how hard the tablets were. Formulation F7 (6% superdisintegrant, 2% binder) had the best profile of all, with a disintegration time of 25 seconds and 98.3% drug release. The study shows that DoE is a good way to optimize the development of strong, patient-friendly FDTs that work well.

ChitosanPLGAEudragit S100NanotechnologyIn Vitro ReleaseDrug Entrapment Efficiency+3 more
6,716 views
2,048 downloads

Contributors:

 S J Shankar
,
 Mrs. Akshatha R S
,
 Mr. Kushal N
,
 Ms. Harshitha Shetty B S
,
 Yashashwini M
Research PaperID: JPRIMS910111

Smart Hydrogels In Controlled Drug Delivery: A Novel Pharmaceutical Approach

A.Bharath r Kumar

Smart hydrogels have emerged as a promising third-generation platform for controlled and targeted drug delivery, offering stimuli-responsive behavior that enables precise spatial and temporal drug release. These hydrophilic polymer networks respond to physiological triggers such as pH, temperature, and enzymatic activity, thereby improving drug bioavailability, therapeutic efficacy, and reducing systemic toxicity. Preclinical studies across various disease models—including cancer, diabetes, inflammatory, and neurological disorders—have shown significant benefits, including sustained drug release, enhanced tissue targeting, and improved safety profiles. Furthermore, integration with nanoparticles and technologies like 3D printing has expanded their functionality, enabling applications in theranostics and personalized medicine. Despite notable advancements, challenges such as reproducibility, biodegradation, regulatory classification, and manufacturing scalability remain barriers to clinical translation. Ongoing research focusing on standardization, biocompatibility, and regulatory alignment is essential to fully realize the potential of smart hydrogels in precision therapeutics.

Drug ReleaseOptimizationParacetamolBinderSuperdisintegrantsDesign of Experiments (DoE)+1 more
7,006 views
2,077 downloads

Contributors:

 A.Bharath r Kumar
Research PaperID: JPRIMS910112

Solid Lipid Nanoparticles for Poorly Soluble Drugs: Formulation and Evaluation

Sujit Ramchandra Deshmukh, Mayuri Shatrughna Ghadge, Ajay vitthal nalawade, Ravindra Raghunath Mahajan

Poor water solubility is still a big problem in medication development since it typically makes oral formulations less bioavailable and less effective at treating diseases. The goal of this project was to create and test solid lipid nanoparticles (SLNs) as a new way to deliver medications that don't dissolve well. Four SLN formulations were made and tested using a hot homogenization followed by ultrasonication method. The tests looked at the size of the particles, the polydispersity index (PDI), the zeta potential, the entrapment efficiency, the drug loading, and the in vitro drug release. The results showed that higher concentrations of surfactants and lipids made the particles smaller, trapped more drugs, and released them over a longer period of time. Formulation F4 had the best performance, with a particle size of 130 nm, an entrapment efficiency of 88%, and a drug release rate of 85% at 24 hours. Statistical analysis showed that there were big differences across the formulations (p

Clinical Translation.Therapeutic EfficacyNanoparticle IntegrationBiocompatibilityPrecision MedicineStimuli-Responsive Polymers+2 more
7,147 views
2,072 downloads

Contributors:

 Sujit Ramchandra Deshmukh
,
 Mayuri Shatrughna Ghadge
,
 Ajay vitthal nalawade
,
 Ravindra Raghunath Mahajan
Research PaperID: JPRIMS910113

Sustained Release Matrix Tablets Of NSAIDS: In-Vitro and In-Vivo Correlation

Akshatha R S, Kushal N, Ms. Alice Patricia A, Harshitha Kumari B A, Varsha A

Non-steroidal anti-inflammatory drugs (NSAIDs) have wide applicability in management of inflammatory and pain related diseases but limited applicability is characterized by common use and gastrointestinal disturbance. Present study is the trying to come up with sustained release (SR) matrix tablets of NSAIDs using hydrophilic and hydrophobic polymers and correlate the results of in-vitro drug release with the in-vivo pharmacokinetics response. The Ibuprofen drug was selected to be the model, and the direct compression of matrix tablet with HPMC K100M and ethyl cellulose was done. The drug was undergone in-vitro dissolution study using USP-II apparatus with phosphate buffer (pH7.2) and during in-vivo pharmacokinetics testing using healthy volunteers approach crossover study. They came up with a favourable Level An in-vitro/ in-vivo correlation (IVIVC) (R 2= 0.987), showing that the in-vitro kinetics of drug released is a fair representation of the average put on plasma. Sustained release matrix has succeeded in prolonging the duration of drug release to 12 hours and reduced Cmax which contributed to reduction of adverse effects related to a peak. These findings encourage studies into establishing the means of developing SR NSAID formulation to assist in GI toxicity and compliance in patients.

BioavailabilityNanotechnologySustained ReleaseEntrapment EfficiencyDrug DeliveryPoorly Soluble Drugs+1 more
6,938 views
2,098 downloads

Contributors:

 Akshatha R S
,
 Kushal N
,
 Ms. Alice Patricia A
,
 Harshitha Kumari B A
,
 Varsha A
Research PaperID: JPRIMS910114

Transdermal Drug Delivery: Advances In Permeation Enhancers and Microneedles

Akshatha R S, Ms. Alice Patricia A, Ms. Ashwini K V, Ms. Harshitha Kumari B A, Varsha A A

Transdermal drug delivery systems (TDDS) is a promising method of non-invasive delivery of drug molecules, and it has the following benefits: it avoids first-pass metabolism, minimizes intestinal breakdown and increases patient compliance. The stratum corneum however presents a great obstacle to drug permeation and more so on hydrophilic and high-molecular-weight drugs. More recent developments have then been directed at the inclusion of chemical permeation enhancers (CPEs) which comprise alcohols, fatty acids, terpenes and surfactants that disturb the structure of the lipids, and increases the solubility of the drug in order to enhance permeation. Simultaneously, the so-called microneedle (MN) technologies, which could be solid, coated, hollow, or dissolving, have been developed to generate the temporary microchannels in the skin and allow deep and efficient drug delivery with low discomfort and minimal damage. Effectiveness, safety, and mechanism of both CPEs and MNs were proven in preclinical trials based on rodent and porcine models, where porcine skin was also compared as a translational-friendly model known to mimic the human one. Noteworthy, the formulation of CPEs with microneedles has demonstrated the synergetic phenomenon, by improving the drug flux, extending therapeutic potential, and extending the ability to deliver a broadened range of molecules such as peptides, hormones, and even vaccines. This review summarizes the existing evidence and points at the translational prospects of the above-mentioned technologies, as well as the future directions of clinical application and improvement of formulation in trans-dermal therapies.

IVIVC (In-vitro/In-vivo correlation).In-vivo pharmacokineticsIn-vitro drug releaseMatrix tabletsSustained release
7,033 views
2,238 downloads

Contributors:

 Akshatha R S
,
 Ms. Alice Patricia A
,
 Ms. Ashwini K V
,
 Ms. Harshitha Kumari B A
,
 Varsha A A