Dr. Hindustan Abdul Ahad received his B. Pharm degree in 1997 from Bangalore University, Karnataka, and his M. Pharm degree in 2001 from Annamalai University in Chidambaram, Tamil Nadu, and his Ph.D. in Pharmaceutical Sciences in 2011 from Jawaharlal Technological University in Hyderabad, Telangana. He received the best researcher award for the years 2019, 2020, and 2021. He has published more than 400 publications in national and international journals, published 11 books and a book chapter and received several awards, including the Best Educationist Award (2015), Best Researcher Award (2019), and many more in his 23 years of experience in academic/research/administrative. He has guided 4 Ph.D. and is currently guiding 7 Ph.D.
EDUCATION
M. Pharm., PhD., FAGE
RESEARCH, TEACHING, or OTHER INTERESTS
General Pharmacology, Toxicology and Pharmaceutics, Pharmaceutical Science, Pharmacology, Toxicology and Pharmaceutics, Pharmaceutical Science
DEVELOPMENT AND IN-VITRO CHARACTERIZATION OF A HPMC K4M AND GUAR GUM-BASED TRIPLE-LAYER MATRIX TABLET SYSTEM FOR CHONDROITIN SULPHATE AND DICLOFENAC SODIUM Hindustan Abdul Ahad, sateesh Kumar Edukulla, Rakesh SP, Thirumalesh Sugali Banoth, Nikhil Kumar Ganugapenta Bulletin of Pharmaceutical Sciences Assiut, 2025 This investigation aimed to make a triple-layer matrix tablet for the oral sustained release of chondroitin (CTN) and diclofenac sodium (DFC) to prolong their therapeutic action. Matrix tablet granules containing CTN and DFC were prepared using wet granulation with Hydroxy propyl methylcellulose (HPMC) K4M and guar gum. A triple-layer tablet structure was fabricated by sequentially compressing three layers: a central layer containing the drug-loaded matrix granules, flanked by two release retardant layers on each side. The retardant layers comprised varying proportions (50-100 mg) of HPMC K4M (X1) and guar gum (X2) as inputs for the responses, cumulative drug release, and swelling index. The physicochemical properties and drug compatibility were evaluated. In-vitro drug dissolution outlines were determined and fitted to numerous mathematical models to elucidate the drug release kinetics and mechanism. The physicochemical evaluations indicated acceptable tablet properties and drug compatibility. Mathematical modeling of the dissolution profiles revealed that the drug release from the matrix tablets was best described by a model indicative of heterogeneous erosion. Formulation F-7, containing 75 mg of HPMC K4M and 39.65 mg of guar gum in the retardant layers, demonstrated the ability to sustain the drug release rate over an extended period. The developed triple-layer matrix tablet system, particularly formulation F-7, offers a promising approach for achieving sustained CTN and DFC oral delivery. The drug release mechanism was known to be predominantly governed by heterogeneous erosion of the matrix. The optimized formulation could enhance patient obedience by reducing the rate of drug administration.
Formulation and Characterization of Simvastatin Transdermal Patches by Central Composite Design Letters in Applied Nanobioscience, 2025 The study aimed to develop transdermal patches containing Simvastatin and evaluate their characteristics and drug release profile. The researchers used the solvent evaporation and tested different polymer ratios and solvents to prepare the patches. They also conducted FTIR studies to ensure compatibility between the drug and excipients. Various parameters were evaluated to assess the quality of the patches. The thickness of the patches ranged from 0.31±0.01 to 0.37±0.02mm, indicating consistency in thickness across different formulations. The weight of the patches varied from 0.29±0.02 to 5.01±0.02mg, reflecting the various amounts of drug and excipients in each formulation. The folding endurance values, which indicate the ability of the patches to withstand repeated folding without breaking, ranged from 253±3 to 289±2, suggesting good mechanical strength. In vitro diffusion studies were conducted to measure the release of Simvastatin from the patches over time. The cumulative percentage of drug release after 74 hours ranged from 82.3% (F8) to 85.7% (F6) for the transdermal films. The formulation F6 exhibited a higher drug release percentage than F8, indicating a more rapid and sustained release of Simvastatin. Based on the results, the researchers concluded that formulation F5 demonstrated favorable characteristics, such as appropriate thickness, weight, folding endurance, and in vitro drug diffusion. However, it is essential to note that additional studies, including in vivo evaluations and stability testing, would be necessary to assess the potential of the transdermal patches containing Simvastatin fully.
Azadirachta indica Fruit Mucilage Aided Mucoadhesive Microspheres of Acyclovir for Drug Entrapment and Mucoadhesive Time Assets with Design-Expert Software Gorantla Naresh Babu, Menaka M Menaka, Hindustan Abdul Ahad Indian Journal of Pharmaceutical Education and Research, 2025 Introduction: Mucoadhesive microspheres for drug delivery are retained in the stomach for an extended period for localized drug release and effect. Objectives: This research aims to explore the mucoadhesive properties of Azadirachta indica fruit mucilage when incorporated into mucoadhesive microspheres, utilizing Acyclovir as a model drug. Materials and Methods: Employing a Box Behnken design, 13 formulations of microspheres were developed, varying Azadirachta indica Mucilage (AIFM) levels, carbomer 934P and stirring speed. Design Expert software was used to assess the impact of these factors on entrapment efficacy and mucoadhesion time. Congeniality studies involved the examination of microspheres for Acyclovir content and discharge. Results: Results indicated that Acyclovir entrapment increased with higher AIFM levels and mucoadhesion time was prolonged in formulations with elevated AIFM levels. The optimal stirring speed was determined to be 750 rpm. Conclusion: The study concludes that Acyclovir demonstrates effective stomach-specific drug delivery through carbomer 934P, further enhanced by Azadirachta indica fruit mucilage, particularly at a stirring speed of 750 rpm in the formulation of mucoadhesive microspheres.
Optimization of Vildagliptin Delivery: Formulation and Evaluation using Box-Behnken Design Ranjitha Venkatesh, Hindustan Abdul Ahad, E Sateesh Kumar Research Journal of Pharmacy and Technology, 2024 The presented study focuses on creating and assessing an in situ gastro-retentive gel designed to deliver Vildagliptin accurately to the stomach. The primary objective is to prolong residence time and enhance drug delivery at the targeted site. The synthesis of these gels in situ utilized a cation-controlled gelation method, incorporating various blends and levels of pectin and HPMCK4M. A thorough evaluation encompassed multiple parameters, including visual appearance, pH values, viscosity, in vitro gel formation, in vitro buoyancy, drug content, density, gel force, water absorption, and in vitro drug release. These gels exhibited a total float time exceeding 12 h, with a float delay time of < 2 min. Formulation T-4, characterized by higher levels of pectin and HPMCK4M demonstrated promising cumulative drug discharges of 96.70±3.28%, over 12h. Subsequent in vitro dissolution and stability studies verified consistent active ingredient content, underscoring the stability of the formulations. In summary, the study underscores the efficacy of the developed in situ gels in prolonging gastric residence time, enabling controlled and sustained discharge of Vildagliptin in the stomach, suggesting potential advancements in drug delivery systems.
Profession for the Magnitude of Temperature and Exposure time on Opuntia elatior cladode extraction on percent yield using design expert software Hindustan Abdul Ahad, Mazin Aboobaida Abdalla Abdelaziz, Hossamaldeen Bakrey, Abdulkadir Abdu, Yassin Babkir Elshiekh Mohamed, Amal. A. Noureldeen Research Journal of Pharmacy and Technology, 2023 The drive of the currentexamination is to decide the consequence of temperature and duration on Opuntia elatior cladodes extraction. The literature claims that little attempt was made to extract from cladodes and other plant parts. The effect of dependent factors on the independent response was not attempted to be screened for. The effect of the dependent variable on the answer was controlled during the experiment's design by the Design Expert. The effect of independent variables (temperature and exposure duration) on the response (% yield) could also be evaluated by positioning, authenticating, and hauling out samples in the water. The extraction and exposure times are directly proportional, and the research found that 40°C is the best temperature for removing the substance from cladodes.
INNOVATIVE APPROACHES TO ENHANCE GASTRIC RETENTION OF RABEPRAZOLE USING Macrocystis pyrifera EXTRACT Pynskhemlin Syiemlieh, K.S. Srilatha, Hindustan Abdul Ahad, Chrishmitha Sequeira, Becare Dkhar, John Mithi Applied Biological Research, 2023 The work aimed to formulate and assess floating tablets of Rabeprazole (RBZ) for treating peptic ulcers. Effervescent tablets were produced (F1-F9) with variations in the concentration of synthetic polymer HPMC K15 for F1, F2, and F3; natural polymer Macrocystis pyrifera extract (sodium alginate) for F4, F5, and F6; and combinations of these polymers for F7, F8, and F9. The research involved several stages, including pre-formulation studies of the pure drug. The tablets were assessed for compatibility, pre-formulation, and post-formulation studies. The compatibility study indicated that there were no interfaces between drug and polymers. The floating tablets passed all the pre- and post-compression constraints. Among them, F6 exhibited a drug content of 99.67 ± 0.11% and sustained drug release over 8 h. All formulations displayed favorable floating behaviour and remained afloat for more than 24 h. The study concludes that a combination of synthetic (HPMC K15) and natural (Macrocystis pyrifera extract) polymers found to extend the RBZ residence time in the stomach and achieve sustained drug discharge. This approach could hold promise for improving the treatment of peptic ulcers.
Quality by Design based Quercetin Hydrate Nanoemulsions for Enhanced Solubility by Reducing Particle Size Lakavath Sunil Kumar, Hindustan Abdul Ahad Indian Journal of Pharmaceutical Education and Research, 2023 Abstract: Aim/Background: The oral-based drug delivery system has a great pace in this era of novel discoveries. The globe is running toward new medical dosage forms, but from the primer days of drug discovery to now, a major issue faced by pharmaceutical scientists is solubility and bioavailability issues. The nanoemulsions are the best suitable formulations which can upsurge the bioavailability of the insoluble drugs. In the past three years, many research activities have been conducted due to the pandemic situation. Almost all nations have concentrated on scientific and medical research during this process. Materials and Methods: In recent days, quercetin hydrate has been found to have anti-malarial activity for which the bioavailability can be uplifted by using Nanoemulsion formulations. The authors used the high-energy process for formulating the nanoemulsions with the support of design expert software, where it was easy to find the number of trials to be performed. Various tools are used for the optimization of formulations for novel drug delivery systems. These tools have been found advantageous as they lead to a reduction in the number of experiments and less wastage of costly reagents. The purpose of the selection of a Central Composite Design (CCD) was that it required fewer runs over various other designs. Results: According to the design expert, CCD software was accessible for 17 runs, which corresponded to 17 groupings or formulations. Batches produced by the experimental design were formulated and assessed for globule size and dispersibility. Conclusion: Even though quercetin hydrate has been approved as a remedy for the treatment of various disorders, its poor oral bioavailability due to poor aqueous solubility and variable absorption is still a challenge in its clinical applications. Quercetin hydrate-loaded nanoemulsion fabricated with Opuntia ficus indica seed oil, PEG400, tween 80, and ethanol resulted in getting nano-sized particles that help in drug solubility and bioavailability. This work illustrated the importance of nanoemulsion to enhance the bioavailability of Quercetin hydrate. Keywords: Quercetin hydrate, Bioavailability, Design expert, Globule size, Nanoemulsion.
Central Composite Design Assisted Formulation Development and Optimization of Gastroretentive Floating Tablets of Dextromethorphan Hydrobromide Haranath Chinthaginjala, Hindustan Abdul Ahad, Sainath Kethandapatti Srinivasa, Srihith Roy Yaparla, Snehitha Buddadasari, Junaid Abul Hassan, Sai Sree Pullaganti Indian Journal of Pharmaceutical Education and Research, 2023 Objectives: The existing study is concerned with the formulation and optimization of dextromethorphan hydrobromide floating tablets via central composite design. Materials and Methods: Direct compression method was employed to prepare the tablets. Drug -excipient studies were executed through FT-IR and DSC analysis. The independent variables selected were the concentrations of Carbopol 934 (X 1 ) and HPMC K15M (X 2 ). The dependent variables designated were Floating Lag Time (FLT) and Drug Release (DR) at 12 hr. The model was found to be nonlinear and the curvature effect was significant. Hence, the system suggested to central composite design. Results: FT-IR studies demonstrated that there is no considerable interaction amid the drug and the excipients. DSC studies revealed that drug and excipient were compatible as there is no significant alteration in melting point of drug when blended with excipients. The precompression parameters of the formulations showed good flow properties. The evaluation of post compression parameters indicated that all the prepared formulations were within the specified limits. Floating lag time of formulations were marked to be less than 1 min and total floating time exceeding 12 hr. Percentage drug release of all formulations were in the range of 89.7% to 99.4%. The obtained design space/contour plots were used for selecting batches in desirable ranges. Conclusion: The results revealed that experimental design was successfully used to optimize polymer concentrations. It was determined that the central composite design would be used to formulate dextromethorphan gastroretentive floating tablets with fewer trials and higher quality features.
Impact of Pistacia lentiscus Plant Gum on Particle Size and Swelling Index in Central Composite Designed Amoxycillin Trihydrate Mucoadhesive Microspheres Sowjanya Hatthi Belgal Mundarinti, Hindustan Abdul Ahad Indian Journal of Pharmaceutical Education and Research, 2023 Abstract: Objectives: The ambition of this study is to find the mucoadhesive assets of Pistacia lentiscus plant gum (mastic gum) by combining it into mucoadhesive microspheres with Amoxicillin Trihydrate (ATH). Significance: Due to its short stomach residence duration, ATH is efficient against H. pylori but can be improved by creating Mucoadhesive Microspheres (MMS) that keep Amoxicillin trihydrate in the stomach. In this study, Pistacia lentiscus plant gum has been exposed to have gastroprotective and H. pylori eradication possessions in inclusion to being able to increase mucoadhesion. Methods and Results: The study was performed to find the influence of the mucilage amount on particle size and swelling index. MMS of ATH (9 batches) were made with carbopol 934P (C-934P) and changeable extents of Pistacia lentiscus plant gum commonly called Mastic Gum (MG). A central composite design to find the influence of factors (MG and C-934 P levels) on particle size and swelling index as an output. The batches were evaluated for their physical limitations, ATH level, and liberation as part of amiability research. The particle size was seen as 35.2±0.3-48.1±0.6μm. In batch B-1, the particle size was the smallest compared to the larger size in B-8. The overall formula was +47.04+0.6500A+1.93B-0.1750AB-0.6167A²-8.47B². The swelling ranged from 58.6±1.3-74.3±1.6 and it was also observed to increase with the polymer level and the formula was +54.21+1.40A+6.25B+0.4750AB-0.5667A²+2.78B². Conclusion: The search establishes that the particle size and the swelling index depend on Pistacia lentiscus plant gum levels. The investigation revealed that ATH was consistently released in a regulated pattern and that encapsulation efficiency, mucosal adhesion, ATH content, and other limitations were considered good. When prepared as an MMS, ATH can achieve good gastric-specific drug delivery when enriched with MG and C-934P. The microspheres had smooth surfaces and were found to be spherical by scanning electron microscopy. Keywords: Mastic gum, Microspheres, Mucoadhesive, Particle size.
A Review on Enzyme Activated Drug Delivery System Hindustan Abdul Ahad, Chinthaginjala Haranath, Srikantham Sai Vikas, Naga Jyothi Varam, Tarun Ksheerasagare, Surya Prakash Reddy Gorantla Research Journal of Pharmacy and Technology, 2021
Synthesis and Molecular Docking Studies of Some 1,2-Dimethyl-3(4-substituted phenyl-1,3-thiazol-2-yl)2,3-dihydroquinazolin-4(1H)-ones as Anticancer Agents Indian Journal of Heterocyclic Chemistry, 2020
Rapid and sensitive bioanalytical method development and validation for quantification of metoprolol using LC-MS/MS in human plasma Journal of the Chemical Society of Pakistan, 2020
Challenging Protection for Geographical Indications: The Distinct Intellectual Property Right Based on Local Knowledge and Reputation Pharma Times, 2020
Designing and characterizing of tramadol hydrochloride transdermal patches prepared with Ficus carica fruit mucilage and povidone Pakistan Journal of Pharmaceutical Sciences, 2016
Method development and validation of a simple uv spectrometric method for the quantification of irbesarton in bulk and its tablets International Journal of Research in Pharmaceutical Sciences, 2016
Stability indicating method development and validation for simultaneous estimation of amitriptyline hydrochloride and chlordiazepoxide by RP-HPLC Journal of Global Trends in Pharmaceutical Sciences, 2015
Formulation and evaluation of sustained release matrix tablets of ciprofloxacin HCL using gum kondagogu and chitosan as matrix forming polymers International Journal of Pharmaceutical Sciences Review and Research, 2014
Development of RP-HPLC method for rapid determination of metaxalone and in bulk and its solid oral dosage form International Journal of Chemical Sciences, 2014
Novel approach in designing mouth dissolving tablets of cetirizine hydrochloride Indian Journal of Pharmaceutical Education and Research, 2012
Preparation of glimepiride sustained release matrix tablets using Hibiscus rosa-sinensis leaves mucilage and povidone Indian Journal of Pharmaceutical Education and Research, 2012
Fabrication and in vitro evaluation of high density gastro retentive microspheres of Famotidine with synthetic and natural polymers Indian Journal of Pharmaceutical Education and Research, 2012
A novel mucilage from Ficus glomerata fruits for transdermal patches: Taking indomethacin as a model drug Iranian Journal of Pharmaceutical Sciences, 2011
Formulation and evaluation of Ficus glomerata mucilage sustained release matrix tablets of gliclazide Pakistan Journal of Pharmaceutical Sciences, 2011
Novel approach in designing and In-vitro evaluation of mouth dissolving tablets of metoclopramide hydrochloride Der Pharmacia Lettre, 2011
preparation and evaluation of Glipizide Azadirachta indica fruit mucilage Poly Vinyl Pyrrolidone sustained release matrix tablets Der Pharmacia Lettre, 2011
Fabrication and evaluation of Gliquidone Azadirachta indica fruit mucilage and Poly Vinyl pyrrolidone sustained release matrix tablets Der Pharmacia Lettre, 2011
Novel approach in designing of mouth dissolving tablets for bitter drugs: Taking clozapine as model drug Der Pharmacia Lettre, 2011
Formulation and in-vitro evaluation of Glimepiride and Parecoxib combination mucoadhesive tablets Der Pharmacia Lettre, 2011
Fabrication and in vitro evaluation of gliquidone matrix tablets with abelmoschus esculentus fruit mucilage and povidone combination Acta Pharmaceutica Sciencia, 2011
Development and in vitro evaluation of glibenclamide aloe barbadensis miller leaves mucilage controlled release matrix tablets International Journal of Pharmtech Research, 2010
Permeation studies of Diclofenac sodium From Ficus carica fruit mucilage matrices for transdermal delivery International Journal of Pharmtech Research, 2010
Permeation studies of diclofenac sodium from ficus carica fruit mucilage matrices for transdermal delivery International Journal of Chemtech Research, 2010
Formulation and evaluation of once-daily sustained release Aceclofenac Prosophis juliflora gum matrix tablets International Journal of Pharmaceutical Sciences Review and Research, 2010
Designing and evaluation of Diclofenac sodium sustained release matrix tablets using Hibiscus rosa-sinensis leaves mucilage International Journal of Pharmaceutical Sciences Review and Research, 2010
Characterization and permeation studies of Diltiazem hydrochloride-Ficus reticuleta fruit mucilage transdermal patches International Journal of Pharmaceutical Sciences Review and Research, 2010
Designing and evaluation of glimepiride Ficus glomerata fruit mucilage matrix transdermal patches Asian Journal of Chemistry, 2010
Formulation and evaluation of glimepiride Cordia dichotoma G. Forst fruit mucilage sustained release matrix tablets Asian Journal of Chemistry, 2010
Formulation and evaluation of aloe barbadensis miller mucilage based controlled release matrix tablets of glimepiride Asian Journal of Chemistry, 2009
RECENT SCHOLAR PUBLICATIONS
Harnessing liposome technology for precision medicine: design, delivery, and clinical impact G Nikhil Kumar, E Satheesh Kumar, TNS Banoth, A Sugunarajan Latha, ... Nanomedicine Journal 13 (2), 283-295 , 2026 2026
Development and In Vitro Characterization of a HPMC K4M and Guar Gum-Based Triple-Layer Matrix Tablet System for Chondroitin Sulphate and Diclofenac Sodium H Abdul Ahad, R SP, T Sugali Banoth, NK Ganugapenta Bulletin of Pharmaceutical Sciences Assiut University , 2025 2025
Innovative Cloud Solutions: Reshaping the Future of Healthcare and Pharma Industries with Enhanced Efficiency, Collaboration and Patient-Centric Paradigms R Venkatesh, HA Ahad, A Sreedhara, SR Gowda, C Krishnappa, ... Asian Journal of Pharmaceutical Research 15 (2), 163-170 , 2025 2025 Citations: 2
Azadirachta indica Fruit Mucilage Aided Mucoadhesive Microspheres of Acyclovir for Drug Entrapment and Mucoadhesive Time Assets with Design-Expert Software. GN Babu, M Muthukaruppan, HA Ahad Indian Journal of Pharmaceutical Education & Research 59 , 2025 2025 Citations: 1
In Vivo Pharmacokinetic Evaluation of a Gastro-retentive Triple Drug Delivery System Utilizing Natural Polymers for Enhanced Helicobacter pylori Eradication E Satheesh Kumar, HA Ahad Bulletin of Faculty of Pharmacy Cairo University 63 (1), 6 , 2025 2025
ADVANCEMENTS IN OPTIMIZING MICROSPHERE PREPARATION: A COMPREHENSIVE REVIEW OF PAST RESEARCH UTILIZING FACTORIAL DESIGN METHODOLOGY HA AHAD, AC KOTIAN, P PRASAD ADVANCES IN PHARMACOLOGY 13 (2), 168-181 , 2025 2025
Harnessing Azadirachta indica fruit mucilage in mucoadhesive microspheres for effective viral infection mitigation: Design-Expert guided optimization ES Kumar, HA Ahad RGUHS J Pharm Sci 15 (1), 8-15 , 2025 2025 Citations: 3
Enhancing environmental health: The role of chemical flocculation in wastewater remediation R Singh, HA Ahad, SP Rakesh, GN Kumar, PR Mohanraja, G Jyotheesh Research Journal of Pharmaceutical Dosage Forms and Technology 17 (1), 41-52 , 2025 2025
Charting the path of success: A deep dive into microspheres-A comprehensive review for researchers uncovering triumphs, innovations and future directions SR Gowda, HA Ahad, ES Kumar, A Sreedhara, R Venkatesh Asian Journal of Research in Pharmaceutical Sciences 14 (4), 391-400 , 2024 2024
A Deep Dive into Microspheres-A Comprehensive Review for Researchers Uncovering Triumphs, Innovations and Future Directions SR Gowda, HA Ahad, ES Kumar, A Sreedhara, R Venkatesh Asian Journal of Research in Pharmaceutical Science 14 (4) , 2024 2024 Citations: 1
Exploring Travel Medicine Perspectives among Primary Care Physicians in Kurnool District: A Comprehensive Study of Knowledge, Attitudes, and Practices RR Satharla, HA Ahad Archives of Medicine and Health Sciences 12 (2), 160-166 , 2024 2024
An Outbreak of the Monkeypox Virus: An Alert to Mankind RM Naik, HA Ahad, H Chinthaginjala, B Varalakshmi, S Dheeraj, PJ Sree Asian Journal of Research in Pharmaceutical Sciences 14 (1), 11-18 , 2024 2024 Citations: 1
An Alert to Mankind RM Naik, HA Ahad, H Chinthaginjala, B Varalakshmi, S Dheeraj, ... Asian Journal of Research in Pharmaceutical Science 14 (1) , 2024 2024
Optimization of vildagliptin delivery: formulation and evaluation using box-behnken design R Venkatesh, HA Ahad, ES Kumar Research Journal of Pharmacy and Technology 17 (12), 5923-5930 , 2024 2024
Breaking barriers in ocular drug delivery: Unveiling the role of ocular inserts as controlled release systems S Panchal, HA Ahad, H Srinivas, GB Ramachandra, M Gangadharaiah, ... Research Journal of Pharmaceutical Dosage Forms and Technology 16 (3), 245-250 , 2024 2024 Citations: 1
Navigating the Global Landscape: A Comprehensive Review of Bower and Sulez's Strategic Insights in the Pharmaceutical Industry R Aishwarya, HA Ahad, S Varsha, V Ranjitha Research Journal of Pharmaceutical Dosage Forms and Technology 16 (1), 51-54 , 2024 2024 Citations: 2
Nanostructured lipid carriers: a potential era of drug delivery systems H Chinthaginjala, V Bogavalli, AA Hindustan, J Pathakamuri, ... Ind. J. Pharm. Edu. Res 58 (1), 21-33 , 2024 2024 Citations: 16
Profession for the Magnitude of Temperature and Exposure time on Opuntia elatior cladode extraction on percent yield using design expert software HA Ahad, MAA Abdelaziz, H Bakrey, A Abdu, YBE Mohamed, ... Research Journal of Pharmacy and Technology 16 (12), 5760-5764 , 2023 2023 Citations: 2
Out-of-trend statistics in the pharmaceutical industry: A gain leap in assuring the quality of the product D Mamatha, HA Ahad, G Ushasree, K Vinod, C Haranath, P Kiran Asian Journal of Research in Chemistry 16 (6), 423-428 , 2023 2023 Citations: 1
In Vivo Pharmacokinetic Studies of Acyclovir Gastro Retentive Mucoadhesive Microspheres Aided by Azadirachta indica Fruit Mucilage GN Babu, M Menaka, HA Ahad, S Veerabomma Research Journal of Pharmacy and Technology 16 (10), 4554-4558 , 2023 2023 Citations: 4
MOST CITED SCHOLAR PUBLICATIONS
Determining the best poloxamer carrier for thiocolchicoside solid dispersions H Annepogu, HA Ahad, D Nayakanti Turkish Journal of Pharmaceutical Sciences 17 (4), 372 , 2020 2020.0 Citations: 35
Characterization and permeation studies of Diltiazem hydrochloride-ficus reticuleta fruit mucilage Transdermal patches HA Ahad, CS Kumar, BV Ravindra, CGS Sasidhar, G Ramakrishna, ... Int J Pharm Sci Rev Res 1 (2), 32-7 , 2010 2010.0 Citations: 33
Past Decade Work Done On Cubosomes Using Factorial Design: A Fast Track Information for Researchers..(2021) Y Shravani, HA Ahad, C Haranath, B gari Poojitha, S Rahamathulla, ... Int. J. Life Sci. Pharma Res 11 (1), P124-135 , 0 Citations: 33
Equator assessment of nanoparticles using the design-expert software AH Abdul, AG Bala, H Chintaginjala, SP Manchikanti, AK Kamsali, ... International Journal of Pharmaceutical Sciences and Nanotechnology (IJPSN … , 2020 2020.0 Citations: 32
Fabrication Of Glimepiride Datura Stramonium Leaves Mucilage And Poly Vinyl Pyrrolidone Sustained Release Matrix Tablets: In Vitro Evaluation AA Hindustan, UA Babu, K Nagesh, DS Kiran, KB Madhavi Kathmandu university journal of science, engineering and technology 8 (1), 63-72 , 2012 2012.0 Citations: 32
Nanosuspension as Promising and Potential Drug Delivery: A Review. 2020 H Chinthaginjala, H Abdul, APG Reddy, K Kodi, SP Manchikanti, ... Int J Life Sci. Pharm Res 11 (1), P59-66 , 2020 2020.0 Citations: 31
Development and in vitro evaluation of glibenclamide Aloe barbadensis miller leaves mucilage controlled release matrix tablets B Reddy, A Chandra Shekar, BV Ravindra, S Lakshmi Venkatnath Development 2 (2), 1018-1021 , 2010 2010.0 Citations: 31
Designing and evaluation of Diclofenac sodium sustained release matrix tablets using Hibiscus Rosa-Sinensis leaves mucilage HA Ahad, CS Kumar, K Kumar, BV Ravindra, CGS Sasidhar, C Abhilash Int J of Pharm Sci Rev and Res 1 (2), 29-31 , 2010 2010.0 Citations: 27
Central composite design aided formulation development and optimization of clarythromycin extended-release tablets H Chinthaginjala, HA Ahad, E Bhargav, B Pradeepkumar Indian J Pharm Educ Res 55 (2), 395-406 , 2021 2021.0 Citations: 24
Isolation and physicochemical characterization of Ficus reticulata fruit mucilage HA Ahad, J Sreeramulu, VH Bindu, P Ramyasree, BS Padmaja, ... International Journal of Green Pharmacy (IJGP) 5 (2) , 2011 2011.0 Citations: 23
Overview on recent optimization techniques in gastro retentive microcapsules by factorial design HA Ahad, C Haranath, D Rahul Raghav, M Gowthami, V Naga Jyothi, ... Int J Pharm Sci Res 10 (9), 247-54 , 2019 2019.0 Citations: 22
Designing and characterizing of tramadol hydrochloride transdermal patches prepared with Ficus carica fruit mucilage and povidone. HA Ahad, BM Ishaq, M Shaik, F Bandagisa Pakistan Journal of Pharmaceutical Sciences 29 (3) , 2016 2016.0 Citations: 22
Fabrication and in vitro evaluation of glimepiride Hibiscus esculentus fruit mucilage sustained release matrix tablets. HA Ahad, V Rajesh, MVR Gupta, DN Lasya, N Harish, M Khamartaz 2010.0 Citations: 22
Gas generating floating tablets: A quick literature review for the scholars S Kousar, HA Ahad, H Chinthaginjala, P Babafakruddin, J Lakunde, ... Asian Journal of Research in Chemistry 15 (2), 171-175 , 2022 2022.0 Citations: 21
Formulation and in vitro evaluation of gastroretentive ofloxacin floating tablets using natural polymers H Chinthaginjala, HA Ahad, B Pradeepkumar, KS Gandhi, ... Research Journal of Pharmacy and Technology 14 (2), 851-856 , 2021 2021.0 Citations: 21
Exfoliation technique of composing and depictions of clopidogrel bisulphate afloat microspheres SS Harsha, HA Ahad, C Haranath, RR Dasari, M Gowthami, NJ Varam, ... Journal of Evolution of Medical and Dental Sciences 9 (14), 1156-61 , 2020 2020.0 Citations: 20
Formulation and in vitro evaluation of floating tablets of dicloxacillin sodium using different polymers H Chinthaginjala, CB Gandla, MR Challa, B Pradeepkumar, HA Ahad Journal of Young Pharmacists 11 (3), 247 , 2019 2019.0 Citations: 20
Isolation and physicochemical characterization of Hibiscus rosasinensis leaves mucilage HA Ahad, P Yesupadam, P Ramyasree, B Suma Padmaja, M Sravanthi, ... International journal of current research 3 (4), 210-212 , 2011 2011.0 Citations: 20
Permeation studies of diclofenac sodium from Ficus carica fruit mucilage matrices for transdermal delivery. HA Ahad, CS Kumar, BA Kumar, BA Reddy, AC Shekar, NRV Sagar International Journal of ChemTech Research 2 (2), 937-941 , 2010 2010.0 Citations: 19
Fabrication and evaluation of glimepiride Cordia dichotoma G. Forst fruit mucilage sustained release matrix tablets HA Ahad, BP Kumar, C Haranath, KS Reddy Int J Chem Sci 7 (4), 2555-2560 , 2009 2009.0 Citations: 19