Hindustan Abdul Ahad

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

Scopus Publications

Formulation and Characterization of Simvastatin Transdermal Patches by Central Composite Design
AMG Transcend Association
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, and Hindustan Abdul Ahad
Manuscript Technomedia LLP
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, and E Sateesh Kumar
A and V Publications
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, and Amal. A. Noureldeen
A and V Publications
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, and John Mithi
Diva Enterprises Private Limited



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, and Sai Sree Pullaganti
EManuscript Technologies
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.


Quality by Design based Quercetin Hydrate Nanoemulsions for Enhanced Solubility by Reducing Particle Size
Lakavath Sunil Kumar and Hindustan Abdul Ahad
EManuscript Technologies



Impact of Pistacia lentiscus Plant Gum on Particle Size and Swelling Index in Central Composite Designed Amoxycillin Trihydrate Mucoadhesive Microspheres
Sowjanya Hatthi Belgal Mundarinti and Hindustan Abdul Ahad
EManuscript Technologies



A competent review of computer imitations of pharmacokinetic and pharmacodynamic arrangements




In Vivo Pharmacokinetic Studies of Acyclovir Gastro Retentive Mucoadhesive Microspheres Aided by Azadirachta indica Fruit Mucilage
Gorantla Naresh Babu, Menaka M, Hindustan Abdul Ahad, and Sreedhar Veerabomma
A and V Publications
The study's main goal is to test gastro retentive mucoadhesive Acyclovir (ACR) microspheres for various in vivo characteristics as a follow-up to the work done by Naresh et al (2022). The optimized ACR Azadirachta indica mucoadhesive microspheres (AAMM) were evaluated in vitro using a variety of parameters. Based on previous research findings, the authors used formula-8 (AAMM-8) for in vivo testing. The availability of plasma drugs was tested on six healthy rabbits of both sexes (weighing 2.-2.5kg). By using a parallel design, they were haphazardly parted into two groups of similar size. Later, the study involved HPLC analysis of the drug in the plasma, which required the fabrication of a spiked plasma sample and the development of an analytical procedure (a simple and cost-effective method for ACR).Pharmacokinetic parameters were measured in plasma samples. The study revealed that in vivo animal studies in rabbits showed good levels of ACR. After a single dose of formulation AAMM-8 (8.85mg/kg), the symmetrical mean Cmax values of formulation AAMM-8 (24.36±0.84µg/mL of ACR), were higher than those of ACR. The tmax values of the AAMM-8 were found to be 6 h. The AUC (0-10h) values were observed to be 176.0µg.h/mL, whereas (AUC)0-∞ was observed to be 248.5µg. h/mL. The AUMC readings were observed to be 724.62µg.h/mL. According to the findings, ACR reached systemic circulation faster than pure medication and had acceptable kinetic values.


Hylocereus undatus fruit extraction on percent yield using Design-Expert software: a revelation for the enormousness of temperature and contact time
HindustanA Ahad, Haranath Chinthaginjala, Ksheerasagare Tarun, GummadisaniG Reddy, AdamA.O Adam, AbdelrahamanI Ali, and JyothiV Krishna
Medknow
Background Dragon fruits (Hylocereus undatus) are popular edible fruits of desert and dry-land origin. They are rich in constituents. An attempt was made to find the optimum temperature and duration of exposure for the effective extraction of content from the fruits using Design-Export software. Aim This study aims to see what effect temperature and duration have on dragon fruit (H. undatus) extraction. According to the literature, numerous attempts have been made to extract components from fruits and other plant parts. Materials and methods The authors made an attempt to check if independent variables had an effect on the dependent response. The Design-Expert software was used to control the impact of the independent variable on the response during the experiment’s design. Alternatively, samples were positioned, authenticated, and hauled out into the water, with independent factors (temperature and exposure time) affecting the response (percent yield). Results and conclusions According to the study, 40°C is the ideal temperature to extract the substance from the fruits, and the extraction and exposure times are directly proportional.


A possible alternative to Opiorphin and its stable analogues for treating fibromyalgia pain: A clinical hypothesis
Debaraj Roy
Kare Publishing
The work aimed to explore the clinical hypothesis on the possible alternative to Opiorphin and its stable analogues for treating fibromyalgia pain. Fibromyalgia is a condition characterized by chronic pain triggered by an interplay of biological and psychosocial variables, although the exact pathogenesis is still controversial. Standard therapy for low threshold tender point pain includes NSAIDs and opioid analgesics, both of which have serious adverse profiles after long-term exposure, highlighting the need for an intermediate compound capable of bridging the gap between NSAIDs and opioid analgesics. Opiorphin is an anti-nociceptive modulator which inhibits the enzyme responsible for the degradation of natural endogenous opioid neuropeptides. This paper hypothesizes and concludes that Opiorphin and its stable analogues (Sialorphine, STR-324) can be an alternative for the treatment of chronic long-standing low-threshold tender point pain associated with fibromyalgia.


Impact of Azadirachta indica Fruit Mucilage on particle size and swelling index in Central Composite Designed Acyclovir mucoadhesive microspheres
Gorantla Naresh Babu, Menaka Muthukaruppan, and Hindustan Abdul Ahad
College of Science for Women
The drive of this exploration is to investigate the mucoadhesive assets of A. indica (Azadirachta indica) fruit mucilage by incorporating it into mucoadhesive microspheres with Acyclovir (AVR) as a model drug. The study was performed to check the impact of the mucilage proportion on particle size and swelling index. Nine batches of AVR mucoadhesive microspheres were made with varying proportions of Polyacrylic acid 934P and A. indica fruit mucilage (AIFM). A central composite design with design expert software to check the impact of dependent variables (A. indica mucilage and Polyacrylic acid 934 P levels) on particle size and swelling index as a response. As part of congeniality studies, the batches were examined for their physical constraints, AVR contents, and liberation. The particle size was found to be 35.2±0.3-48.1±0.6μm. In batch B-1, the particle was least sized compared to the larger size in B-5. The investigation found that the particle size and the swelling index depended on AIFM and Polyacrylic acid proportions. The research discovered that AVR was systematically released in a controlled manner and that the entrapment efficacy, mucoadhesion, drug content, and other constraints were found to be good. Acyclovir is capable of good stomach-specific drug delivery by Polyacrylic acid 934P and enhanced by A. indica fruit mucilage when prepared as mucoadhesive microspheres. Scanning electron microscopy reveals that the microspheres were spherical with a fairly smooth surface.


Fabrication and Preliminary Assessment of Neem Fruit Mucilage as Mucoadhesive Abetting Assets with Methpol-934P for Acyclovir Delivery from Mucoadhesive Microcapsules
Gorantla Naresh Babu, Menaka Muthukarupan, Hindustan Abdul Ahad, and Veerabomma Sreedhar
Oriental Scientific Publishing Company
In this study, we investigated the mucoadhesive properties of neem fruit mucilage by incorporating it into mucoadhesive microcapsules with Acyclovir (ACR). Methpol-934P and Neem fruit mucilage (NFM) was used to construct 12 different mucoadhesive microcapsules. We assessed FTIR and DSC capabilities for compatibility with ACR and NFM. ACR mucoadhesive microcapsules (ANMM) were characterized for mucoadhesion and ACR release Physico-chemical characteristics. CR was found to be compatible with NFM in the research. The entrapment increased as the levels of NFM in the formulations increased, and mucoadhesion time was longer in formulations with higher levels of NFM. As levels of NFM increase in formulations, the release of drugs is slightly reduced. NFM may be responsible for this due to its release retarding properties. An additive of neem fruit mucilage allowed for the retention of ACR after ingestion when a mucoadhesive polymer (methpol 934P) was used.


Recent advances in lipid based nanovesicles for transdermal drug delivery
Chinthaginjala Haranath
Medic Scientific
Lipid based nanovesicles are the formulations which are used for the delivery of hydrophilic, hydrophobic and amphiphilic drugs or compounds. They are very helpful for the drugs which are hydrophilic and irritant drugs that can be encapsulated and delivered to the target site. They are very advantageous over conventional formulations. Lipid based nanovesicular systems will efficaciously help the drugs addressing the issues of solubility and penetration thereby promotes bioavailability. Now a days lipid based nanovesicles for transdermal delivery of drug has become very useful especially for hydrophilic drugs. The use of the nanovesicles for transdermal drug delivery will overcome the drawbacks associated with the route of drug delivery, such as oral and parenteral. Lipid based nanocarriers includes liposomes, transferosomes, ethosomes, niosomes, ufasomes, spinghosomes, pharmacosomes etc., This review article describes the types, formulation methods, evaluation and the research works done on lipid based nanovesicles for transdermal delivery of the drug.


Aquasomes: A novel approach for the delivery of bioactive molecules
Chinthaginjala Haranath
Medic Scientific
In recent years, nanoscience has drug development and has taken a new slant, that have proven difficult with traditional dosage forms in drug delivery.Nanoparticles, liposomes, niosomes, quantum dots and Aquasomes are the examples of nanomaterials are just a few examples of nanobiotechnologically created carrier systems. The nano-particulate self-assembled carrier system is anew approachas well as ideal choice for the administration of drugs. Aquasomes proved to be important drug delivery system of ceramic nanoparticles.These are three-tiered framework composed of a core made of solid crystals and adsorbed biologically active drug molecules are coated with carbohydrates.Aquasomes formulations are typically administered via the intravenous route.Aquasomes have the ability to maintain conformational consistency and have a high level of exposure to the surface, making them ideal for the transportation of molecules made up of peptides as well as vaccine and gene delivery to specific sites.


Optimized Rapid Disintegrating Tablets produced through Central Composite Design
Hindustan Abdul Ahad, Haranath Chinthaginjala, Govardhan Reddy, Aravind Kumar Ganthala, and Tharun Teja Siddhartha
Walter de Gruyter GmbH
Abstract The work is aimed at producing fast disintegrating diclofenac potassium tablets to relieve pain and tenderness by applying a quality-by-design approach. Diclofenac potassium (DP) is of BCS class II and has issues of minimal oral bioavailability. This can be overcome by complexing DP with β-cyclodextrin (β-CD) and sodium starch glycolate (SSG). The attempt was to optimize DP tablets by applying central composite design (CCD). Nine different DP tablet formulations were created and assessed for physicochemical constraints, disintegration time and drug dissolution at the end of 30 min. The separate and mutual consequences of β-CD and SSG on the disintegration time of DP tablets are highly significant (P<0.01). The DP tablets made with β-CD in 150 mg disintegrated rapidly within 39±2 sec, and gave very rapid drug dissolution (96.35±2.36%) at the end of 30 min. These DP tablets (F-8) contain β-CD (150 mg) and SSG at 32.07 mg. The intermittent levels of β-CD and higher levels of SSG gave good dissolution of DP tablets. The polynomial equation linking the response, i.e. disintegration time in sec (Y1) and the levels of β-CD (A) and SSG (B) based on the pragmatic results, is Y1=45-3.14277A- 2.46599B-1.25AB+1.75A2-0.5B2. In contrast, the DP release at the end of 30 min was expressed as Y2 = 88.57 + 4.09333A + 3.27837B + 1.2525AB - 2A2 + 0.8875B2. The study concludes that SSG decreases the disintegration time with its concentration and β-CD concentration ingresses the drug release from the formulation.


A Review on Progressive Trends in Pharmaceutical Nano Emulsions and their Assessment
Lakavath Sunil Kumar and Hindusthan Abdhul Ahad
A and V Publications
This review aimed to deliver the progressive trends and need for research activities in the area of liquid bi-phasic systems i.e., Nano emulsion (NE). These categories of drug delivery system (DDS) are progressive modes for providing and increasing the bioavailability of non-aqueous drugs and the drug which have increased the first-pass metabolism. The NE's can be framed by either high or low energy techniques. High-pressure homogenization, micro fluidization, and ultra-sonication are involved in High energy techniques whereas the phase inversion emulsion forming method and the self-NE method are involved in low energy techniques. High energy techniques are having lower usage when compared to low energy techniques due to their high consumption of energy, hence low energy techniques are more operative and do not need any sophisticated devices. Even though high energy techniques are more suitable for food-grade emulsion as they need a reduced amount of surfactant than low energy techniques. Methods for formulation of NE DDS are overlying in nature, exclusively in the process of low energy techniques. This review gives the eminence of NE'S by comparing previous research carried over it.


The Design of Soft Drugs: Basic Principles, Energetic Metabolite Methods, Approved Compounds, and Pharmaceutical Applications




A Desk-top Literature for Research on Gas Engendering and Low-density Floating Drug Deliery Systems




Bygone Exertion on Mucoadhesive Bilayered Tablets
Hindustan Abdul Ahad, Rahul Raghav Dasari, Chinthaginjala Haranath, Madana Gowthami, Naga Jyothi Varam, and Pandyala Sravanthi
A and V Publications
The point of present writing is gathering past work done on mucoadhesive bilayered tablets. Numerous specialists are getting pulled towards these systems to plan of examinations in the streamlining of medication conveyance frameworks as very few studies were advanced till date. Mucoadhesive system is simple to create, utilize, and easily accessible to evaluate the results. The authors made an adequate attempt to bring a platform on various polymers utilized in the advancement mucoadhesive bilayered tablets.


Liver shielding activity of ficus benghalensis fruit extracts contrary to perchloromethane prompted toxic hepatitis in New Zealand albino rats
Hindustan Abdul Ahad, Chinthaginjala Haranath, Naga Jyothi Varam, Tarun Ksheerasagare, Jyothi Vinay Krishna, and Siddartha Tharun Teja
A and V Publications
The main aim of the present investigation was to explore the Liver shielding of Ficus benghalensis fruit extracts alongside perchloromethane persuaded toxic hepatitis in New Zealand albino rats. The ethanolic extract of the fruits of F. benghalensis (Family: Moraceae) was evaluated for Liver shielding in New Zealand Albino rats with liver mutilation persuaded by perchloromethane. F. benghalensis fruit extract unveiled a momentous Liver shielding consequence by dropping the serum concentrations of alanine aminotransferase (ALT), aspartate aminotransferase (AST), total serum bilirubin (TSB) and malondialdehyde equivalent 500 mg/kg (oral). These biochemical explanations were accompanied by a histopathological assessment of liver segments. The liver shielding of F. benghalensis fruit extracts was comparable to that of a known Liver shielding Liv-52.


Datura stramonium leaves mucilage aided buccoadhesive films of aceclofenac using 3² factorial design with design-expert software
Hindustan Abdul Ahad, Haranath Chinthaginjala, Manchikanti Sai Priyanka, Dasari Rahul Raghav, Madana Gowthami, and Varam Naga Jyothi
EManuscript Technologies
Aim and Objectives: The main motto of this work was to search the additive effect of Datura stramonium leaves mucilage in the making of buccoadhesive film by taking Aceclofenac as a model drug. Materials and Methods: Nine formulations of buccal films were made using Carbopol 934 P and varying proportions of Ethyl Cellulose and D. stramonium leaves mucilage. The films were judged for compatibility studies and physical constraints including Aceclofenac content and discharge. Results: Among the films F-9 containing 1:1 of Aceclofenac and ethyl cellulose; and 1:0.5 ratios of Aceclofenac: D. stramonium leaves mucilage was found to have good Mucoadhesion time (10.5±0.1h) and Bioadhesive strength (5.5±0.2g). The formulation F2 showed the highest % release i.e., 92.85% up to 8 h. Conclusion: The study resolved that buccoadhesive drug delivery system for Aceclofenac with ethyl cellulose aided with D. stramonium leaves mucilage meets the ideal requirement for buccal devices is an efficient approach to surpass the hepatic first-pass metabolism and increase bioavailability.


Designing of dexamethasone sodium phosphate ocular films for madras eye: In vitro and in vivo evaluation
Faculty of Pharmacy and Pharmaceutical Sciences, University of Karachi



Formulation and in vitro evaluation of gastroretentive ofloxacin floating tablets using natural polymers
Haranath Chinthaginjala, Hindustan Abdul Ahad, Bhupalam Pradeepkumar, K. Sainath Gandhi, K. Kalpana, G. Pushpalatha, and K. Sumala
A and V Publications

RECENT SCHOLAR PUBLICATIONS

Enhancing Environmental Health: The Role of Chemical Flocculation in Wastewater Remediation
R Singh, HA Ahad, N Kumar, M PR
Research Journal of Pharmaceutical Dosage Forms and Technology 17 (1), 41-52 2025



Azadirachta indica Fruit Mucilage Aided Mucoadhesive Microspheres of Acyclovir for Drug Entrapment and Mucoadhesive Time Assets with Design-Expert Software
GN Babu, M Menaka, HA Ahad
Indian Journal of Pharmaceutical Education and Research 59 (1s), s243-s255 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



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



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



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



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



An Alert to Mankind
RM Naik, HA Ahad, H Chinthaginjala, B Varalakshmi, S Dheeraj, ...
Asian Journal of Research in Pharmaceutical Science 14 (1) 2024



An Outbreak of the Monkeypox Virus: An Alert to Mankind
RM Naik, HA Ahad, H Chinthaginjala, B Varalakshmi, S Dheeraj, PJ Sree
A & V Publications 14 (1), 11-18 2024



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
A & V Publications 16 (1), 51-54 2024



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



From Concept to Assessment: Creating an Oral In-Situ Gelling System with Sucralfate
P Sahani, KS Srilatha, HA Ahad, SK Sah, B Dkhar, RK Prajapati
KEPES 21 (3), 555-567 2023



Past Work Done on the Matrix Tablets: A Quick Reference for the Research Beginner in Sustained-release Dosage Forms.
HA Ahad, H Chinthaginjala, B Meharajunnisa, N Vandana, R Gudisipalli, ...
International Journal of Pharmaceutical Investigation 13 (3) 2023



Impact of Azadirachta indica Fruit Mucilage on particle size and swelling index in Central Composite Designed Acyclovir mucoadhesive microspheres
GN Babu, M Muthukaruppan, HA Ahad
Baghdad Science Journal 20 (2), 0425-0425 2023



Amelioration Of Atlantia Monophylla In Chronic Unpredictable Stress Induced Depression Like Behaviour In Wistar Rats
MOM Idriss, SHH Sudhan, HAA Chinthaginjala Haranath, KS Reddy, ...
Journal of Pharmaceutical Negative Results, 4225-4227 2023



Pushing Limits: Exploring Torsemide's Potential Through In-Vitro Mucoadhesive Buccal Delivery Characterization.
KM Becare Dkhar, HA Ahad, P Sahani, P Syiemlieh
Journal of Advanced Zoology 44 2023



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
A & V Publications 16 (6), 423-428 2023



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



Innovative Approaches to Enhance Gastric Retention of Rabeprazole Using Macrocystis pyrifera Extract
P Syiemlieh, KS Srilatha, HA Ahad, C Sequeira, B Dkhar, J Mithi
Centre For Advancement Of Applied Sciences 25 (4), 465-474 2023



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

MOST CITED SCHOLAR PUBLICATIONS

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
Citations: 32



Determining the best poloxamer carrier for thiocolchicoside solid dispersions
H Annepogu, HA Ahad, D Nayakanti
Turkish Journal of Pharmaceutical Sciences 17 (4), 372 2020
Citations: 30



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
Citations: 30



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), 32-37 2010
Citations: 30



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
Citations: 26



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
Citations: 24



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
Citations: 22



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
Citations: 22



Designing and evaluation of Diclofenac sodium sustained release matrix tablets using Hibiscus Rosa-Sinensis leaves mucilage
HA Ahad, CS Kumar, K Kumar, S CGS
Int J of Pharm Sci Rev and Res 1 (2), 29-31 2010
Citations: 21



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
Citations: 20



Fabrication and in vitro evaluation of glimepiride hibiscus esculentus fruit mucilage sustained release matrix tablets
HA Ahad, V Rajesh, MV Gupta, DN Lasya, N Harish, M Khamartaz
Int J PharmTech Res 2 (1) 2010
Citations: 20



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), 2555-60 2009
Citations: 19



Formulation and in vitro evaluation of gastroretentive ofloxacin floating tablets using natural polymers
H Chinthaginjala, HA Ahad, B Pradeepkumar, KS Gandhi, K Kalpana, ...
Research Journal of Pharmacy and Technology 14 (2), 851-856 2021
Citations: 18



Formulation and in vitro evaluation of floating tablets of dicloxacillin sodium using different polymers
H Chinthaginjala, GC Barghav, CM Reddy, B Pradeepkumar, HA Ahad, ...
Journal of Young Pharmacists 11 (3), 247 2019
Citations: 18



Preparation of Fluconazole β‐Cyclodextrin Complex Ocuserts: In Vitro and In Vivo Evaluation
H Abdul Ahad, J Sreeramulu, BS Padmaja, MN Reddy, PG Prakash
International Scholarly Research Notices 2011 (1), 237501 2011
Citations: 18



Isolation and physicochemical characterization of Hibiscus rosa-sinensis leaves mucilage
HA Ahad, P Yesupadam, P Ramyasree, B Suma Padmaja, M Sravanthi, ...
International journal of current research 3 (4), 210-212 2011
Citations: 18



Gas generating floating tablets: A quick literature review for the scholars
K Shaik, HA Ahad, H Chinthaginjala, P Babafakruddin, J Lakunde, ...
A & V Publications 15 (2), 171-175 2022
Citations: 17



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
Citations: 17



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
Citations: 17



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
Citations: 17

INDUSTRY EXPERIENCE

1 year