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American Journal of Pharmacy and Health Research

📢 Latest Update: Call for Papers – Special Issue on Pharmacy and Health Research (April 2026 Submission Deadline)

📢 Latest Update: Call for Papers – Special Issue on Pharmacy and Health Research (April 2026 Submission Deadline)

Volume 1, Issue 9 - 2013 (December 2013 Issue 9)

Volume 1 Issue 9 Cover

Issue Details:

Volume 1 Issue 9
Published:Invalid Date

Editorial: December 2013 Issue 9

Welcome to the 2013 issue of American Journal of Pharmacy and Health 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 Pharmacy and Health Research

Articles in This Issue

Showing 9 of 9 articles
Research PaperID: AJPHR19001

A Review On Floating Microspheres As Gastroretentive Drug Delivery System

Manjusha A.Gunjal* Archana K Gaikwad

The real challenge in the development of an oral controlled-release drug delivery system is not just to sustain the drug release but also to prolong the presence of the dosage form within the gastrointestinal tract (GIT) until all the drug is completely released at the desired period of time. Floating drug delivery systems (FDDS) have ability to prolong the gastric residence time after oral administration at proper site and release of drug controlled also useful to achieve desired peak plasma concentration and increase bioavailability. This review specify characteristics as well as evaluation of floating microspheres

FDDSGastric emptying timeBuoyancyin vitro release
8,639 views
2,706 downloads

Contributors:

 Manjusha A.Gunjal* Archana K Gaikwad
Research PaperID: AJPHR19002

Jadwar (Delphinium denudatum): A potent Drug for Various Ailments

Ehsan Rauf

Jadwar, root of Delphinium denudatum is an important central Nervous system active drug of Unani  System of Medicine. The generic name of Jadwar is derived from a Greek word, which means Dolphin, as the nectary resembles the figure of Dolphin. The word Jadwar is Arabic form of Persian Zadwar, which means the great purifier or Antidote. In India Jadwar was named as Nirbisi due to its antidotal properties. In various classical texts, it has been mentioned to be sedative, analgesic, brain and nervine tonic and is recommended for various brain and nervine disorders like epilepsy, tremors, hysteria, atony, numbness, paralysis, morphine dependence. Jadwar is adultered with the root of Beesh (Aconite), a poisonous herb root that may cause death. Ethanolic extract showed antibacterial activity against Corynebacterium diphtheriae, Proteus vulgaris, Salmonella typhi and Klebsilla pneumoniae.

JadwarDelphinium denudatumUnani Medicine
9,118 views
2,606 downloads

Contributors:

 Ehsan Rauf
Research PaperID: AJPHR19003

A Pharmacognostic Study on Salvia Hispanica

Avinash Rangaraju, Uppala Mohan Kumar

Chia seed (Salvia hispanica) is an ancient oilseed used by Mayas and Aztecs as foodstuff. This seed is a natural source of omega-3 fatty acids (α-linolenic acid), soluble and insoluble fibers, and proteins in addition to other important nutritional components, such as vitamins, minerals, and natural antioxidants. Chia can be considered as “functional food” because apart from contributing to human nutrition, chia helps to increase satiety index, prevent cardiovascular diseases, inflammatory and nervous system disorders, and diabetes, among others. Today, chia seed offers a huge potential in the industries of health, food, animal feed, pharmaceuticals, and nutraceuticals, among others, due to its functional components. However, the safety and efficacy of this medicinal food or natural product need to be validated by scientific research. In vivo and clinical studies on the safety and efficacy of chia seed are still limited.  This paper covers the up-to-date research on the identified active ingredients, in vivo and human trials on the health benefit of chia seed, and its current market potential.

Salvia hispanicaScanning electron microscopychia seedsomega 3-fatty acids
8,936 views
2,808 downloads

Contributors:

 Avinash Rangaraju
,
 Uppala Mohan Kumar
Research PaperID: AJPHR19004

Seasonal Variation in Antibacterial Activity of Seaweed Hypnea Valentiae and Its Epiphytic Bacteria

Shunmugiah Mahendran, Rajaiah Sudhakar, Gopalan Mahadevan, Kannathasan Gautam, Shanmugam Saravanan

The seaweed Hypnea valentiae was extracted with solvents hexane, acetone and methanol. In the preliminary screening, hexane extract showed wide spectrum activity against ten human bacterial pathogens. The maximum level inhibition was observed against Escherichia coli, Vibrio parahaemolyticus and Micrococcus luteus and minimum against Vibrio cholerae. The assessment of seasonal variation in antibacterial activity with hexane extract showed higher activity during postmonsoon season followed by summer, premonsoon and monsoon season. The epiphytic bacterial density on surface of Hypnea valentiae was 25 x 103 CFU/cm2. Ten epiphytic bacteria (HV1- HV10) was isolated and the strain HV10 showed higher activity which was identified based on the morphologically and biochemical character as Alcaligenes sp. It was further cultured and the culture supernatant was extracted with hexane, n-butanol and water. The n-butanol extract showed higher activity against Shigella flexneri and minimum against Escherichia coli, Pseudomonas aeruginosa and Streptococcus epidermis. The investigation has proved that seaweed Hypnea valentiae and its epiphytic bacterial strain could be the potential source of bioactive compounds of biomedical importance.

Hypnea valentiaeAntibacterial activityEpiphytic bacteria and Solvents extraction
9,005 views
2,741 downloads

Contributors:

 Shunmugiah Mahendran
,
 Rajaiah Sudhakar
,
 Gopalan Mahadevan
,
 Kannathasan Gautam
,
 Shanmugam Saravanan
Research PaperID: AJPHR19005

Formulation and Characterization of Mouth Dissolving Tablet of Levocetrizine Hydrochloride

Anisree.G S, Nishma Poolat, Femina.K, Anu.V, Rauof.P

Mouth dissolving tablets one of the novel approaches in improving patient compliance. Levocetrizine hydrochloride the non-sedative antihistamine drug commonly used for the treatment of allergic rhinitis. Tablet containing levocetrizine with Doshion P54 (C) resin and different superdisintegrants like Sodium starch glycolate, crospovidone, and polacrilin potassium were used for the manufacturing of tablet. Direct compression technique is used for manufacturing of tablet. Combinations of excipients were incorporated to formulate the tablet. Effect of the combinations were studied to optimize the formulation. Compatibility between the drug and excipients were performed with the help of FTIR spectral analysis. The tablets were evaluated for their hardness, wetting time, disintegrating time and dissolution parameters. It was concluded that the tablets having the combination of drug with Sodium Starch Glycolate  and Polacriline Potassium  met all the evaluation parameters and thus selected as the optimized formulation. The optimized formulation was undergone for stability studies in predicting the shelf-life as per ICH guidelines and proved  for its adequate shelf-life. Key words: Mouth dissolving tablet , Levocetrizine hydrochloride, FTIR, ICH guidelines.

Mouth dissolving tabletLevocetrizine hydrochlorideFTIRICH guidelines.
9,328 views
2,883 downloads

Contributors:

 Anisree.G S
,
 Nishma Poolat
,
 Femina.K
,
 Anu.V
,
 Rauof.P
Research PaperID: AJPHR19006

Targeted Therapy Vs Empirical Therapy in Treating Respiratory Pathogen Associated with Co Morbidity

Dhanya.C.S, C.I.Sajeeth, Kiran.D.R, Deepthi Govindankutty, Sujitha Ravindran

The main aim of the study to evaluate the association between co morbid conditions with respiratory tract infections and assess the targeted therapy in treating respiratory pathogens associated with co morbidity. We performed a prospective observational study, evaluating respiratory tract infectious patients, with or without co morbidity. This study was carried out during June 2013 to October 2013. Among 170 RTIs patients enrolled in the study, in that 11(6.5%) were diagnosed with Cardiovascular diseases, 51(30%) with Endocrine disorders, 9 (5.3%) with Hepatic diseases, 7 (4.12%) patients with Genito urinary diseases, 6 (3.53%) with Autoimmune disorders, 25 (14.7%) with Respiratory diseases, 1 (0.59%) patients with immunocompromised diseases and 10 (5.88%) patients with central nervous system diseases. Among 170 patients, in that 120 (70.59%) RTIs patients with co morbidity and 50 (29.41%) normotensive patients without co morbidity. Antibiotics were given as empirical therapy and targeted therapy RTIs patient with co morbidity, in that 91(53.53%) treated as empirically and 29(17.06%) as targeted therapy. The patients with diabetes mellitus had greater risk of developing RTIs. When a patient reports a RTI with co morbidity, it is necessary to identify and assess the co morbidity so as to prevent further complications and irrational therapy. Hence, for patients with RTIs and co morbidity, it is very essential to perform the culture and sensitivity pattern. Key words: RTIs, Co morbidity, Empirical therapy, Targeted therapy.

RTIsCo morbidityEmpirical therapyTargeted therapy.
9,297 views
2,900 downloads

Contributors:

 Dhanya.C.S
,
 C.I.Sajeeth
,
 Kiran.D.R
,
 Deepthi Govindankutty
,
 Sujitha Ravindran
Research PaperID: AJPHR19007

Assessment of Microbiological Quality and the Anti-Bacterial Traits of Sterile Liquids Used for Medication of Eye and Ear Infections in Bangladesh

Kohinoor Akter Raton, Md. Asif Hossain, Mrityunjoy Acharjee1 and Rashed Noor

Current study endeavored to examine the microbiological quality as well as the anti-bacterial traits of different sterile liquid drops commonly applied for the treatment of eye and ear infections in Bangladesh. Fifteen (15) different types of liquid drops manufactured in different pharmaceutical industries were microbiologically examined through common, traditional and replicable cultural and biochemical tests. Total viable bacterial and fungal load (~101 -104 cfu/ml) showed repugnant contamination of which 7 samples significantly exceeded United States Pharmacopeia (USP) or British Pharmacopeia (BP) limit (

Eye & Ear dropsmicrobiological qualityantimicrobial activitypublic health.
9,316 views
2,912 downloads

Contributors:

 Kohinoor Akter Raton
,
 Md. Asif Hossain
,
 Mrityunjoy Acharjee1 and Rashed Noor
Research PaperID: AJPHR19008

Evaluation of Hepatoprotective Effects of Rauwolfia Vomitoria Extract on Liver Enzymes of Adult Wistar Rats.

DN Ezejindu, CJ Ihentuge, OC Okonkwo

This work is aimed at investigating the hepatoprotective effects of Rauwolfia vomitoria extract on liver enzymes following oral administration. Twenty wistar rats of weights 195 -215kg were divided into four groups designated as A,B,C & D. Group A served as the control and received 0.4ml of distilled water;  the experimental groups B,C &D were orally administered with 0.6ml, 0.75ml and 0.81ml of extract of Rauwolfia vomitoria for twenty eight days. Twenty four hours after the  last administration, the animals were weighed, anaesthetized under chloroform vapour and dissected. The liver tissues were removed and weighed. Blood samples were collected through cardiac puncture using sterile syringes and  needles. Blood for serum preparation was collected into sterile plain tubes and stored in the refrigerator for analysis. The activities of serum aspartate aminotransferase (AST), alanine aminotransferase (ALT) and alkaline phosphotase (ALP) were determined using randox kit method.  The final body weight of the experimental groups (B,C & D) increased significantly (P

Wistar ratsRauwolfia vomitoriaLiver weightBody weightHepatoprotective effects.
9,613 views
2,965 downloads

Contributors:

 DN Ezejindu
,
 CJ Ihentuge
,
 OC Okonkwo
Research PaperID: AJPHR19009

Novel Techniques for the Determination of Cisatracurium Besylate Alone or In the Presence of Its Degradation Product

Nisreen F. Abo- Talib, Ramzia I. El- Bagary, Marwa A.El- Wahab Mohamed

Four simple, accurate and precise methods have been developed and validated for the determination of cisatracurium besylate in bulk and in its pharmaceutical preparation. The first method was a spectrofluorimetric method based on measuring the native fluorescence intensity (FI) of cisatracurium (CIS) in aqueous micellar medium at 317 nm upon excitation at 235 nm in the range of 0.2- 2.2 µg.mL-1. The other three methods were adopted for the determination of the studied drug in the presence of its alkaline degradation product including a spectrophotometric method namely, first derivative of ratio spectra (DD1) in the range of 8-38 µg.mL-1 and two high pressure liquid chromatographic (HPLC) methods, one with diode –array detector (DAD) and the other with fluorescence detector (FLD) in the ranges of 1.0- 40.0 µg.mL-1 and 0.25-20.0 µg.mL-1, respectively. Separation was achieved on Supelco Discovery®C18 column (150 mm x 4.6 mm, 5 µm) and Agilent Zorbax® SB- CN column (50 mm x 4.6 mm, 1.8 µm) for HPLC - DAD and HPLC- FLD methods, respectively. All the proposed methods were validated and successfully applied for the determination of CIS in bulk and in pharmaceutical preparation with good recovery ranges between 99.92- 100.71. The results obtained by applying the proposed methods were statistically analyzed and compared with those obtained by the manufacturer method, and no significant difference was found.          

Cisatracurium besylateDiode-array detectorFluorescence detectorSpectrofluorimetry and First derivative ratio of ratio spectroscopy.
9,861 views
2,918 downloads

Contributors:

 Nisreen F. Abo- Talib
,
 Ramzia I. El- Bagary
,
 Marwa A.El- Wahab Mohamed