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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 10, Issue 12 - 2022 (December 2022 Issue 12)

Volume 10 Issue 12 Cover

Issue Details:

Volume 10 Issue 12
Published:Invalid Date

Editorial: December 2022 Issue 12

Welcome to the 2022 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 3 of 3 articles
Research PaperID: AJPHR1012001

Photobiomodulation efficacy of 808 nm Low Level Laser therapy on Lipopolysaccharide compromised Immune status: An Experimental study in Rats

Richa Rathor, Sukanya Srivastava, Asheesh Gupta, Geetha Suryakumar

ABSTRACTThe current study aimed to assess the efficacy of two unlike laser wavelengths (655 nm and 808 nm) used as photobiomodulation or low-level laser therapy (LLLT) on the immune status in male rats. Sixty-five male Sprague–Dawley rats were considered in the experiments which were further divided into three groups. For all the three groups, LPS (lipopolysaccharide) was used as an immunostimulant and it was administered 5mg/kg via intraperitonially (ip) route for 3 consecutive days. In the first group, 655 nm LLLT (power 150 mW) was investigated against LPS induced immune response. Second group investigated 808 nm LLLT (power 150 mW) against LPS induced immune function. After finding out the better responsive LLLT, third group investigated 808 nm LLLT with different power ie 75 mW and 150 mW. The results indicated that 655 nm LLLT at 150 mW power was not restored LPS associated TNF-? and IL-1? content. While, LPS induced enhance IL-1? and TNF-? level was significantly decreased in 808 nm LLLT group. Further, comparison was studied in 808 nm LLLT at different power ie 150 mW and 75 mW and pro-inflammatory cytokines estimation was quantified. The outcome of the study concluded that 808 nm LLLT has anti-inflammatory activity at 150 mW power. Hence, the further research work is required in this direction to advise that 808 nm LLLT at 150 mW could be considered as a treatment to protect inflammatory diseases. Keywords: Photobiomodulation; low-level laser therapy (LLLT); immune status; 655nm; 808nm; in vivo

Photobiomodulationlow-level laser therapy (LLLT)immune status655nm808nmin vivo
105,510 views
31,601 downloads

Contributors:

 Richa Rathor
,
 Sukanya Srivastava
,
 Asheesh Gupta
,
 Geetha Suryakumar
Research PaperID: AJPHR1012002

Development and Evaluation of Anti Acne Cream Using Extracts of Vitex Negundo and Hibiscus Rosa-Sinensis

Sharma Ayushi, Mukati Sandeep, Koshta Ashok, Malviya Sapna, Kharia Anil

ABSTRACTAcne vulgaris is the most common chronic skin disease of the world. The bacteria responsible for acne are Staphylococcus aureus. So many synthetic products are available in the market for acne treatment including antibiotics, but serious side effects arises due to the long-term use of synthetically prepared anti-acne preparations. Bacterial resistance is the major problem that occurs due to the irrational use of antibiotics, in addition to this skin problem, such as erythema, allergy, sunburn and melanin pigmentation. As from ancient times, natural plant substances have been shown to be promising candidates for acne treatment without side effects. Therefore in the present study, the anti acne cream formulation has been prepared using Vitex negundo (leaves), Hibiscus rosa-sinensis (flower) and Tea Tree Oil (Melaleuca alternifoli). The prepared formulation was evaluated on the basis of greasiness, spreadability, homogeneity, skin irritancy, viscosity, pH, emolliency and stability. The antibacterial study was also performed using a well diffusion technique and results showed that formulation possess sufficient anti bacterial activity. This showed that the optimized formulation has anti-acne properties. Keywords: Anti acne, Staphylococcus aureus, Vitex negundo, Hibiscus rosa-sinensis, Melaleuca alternifolia.

Anti acneStaphylococcus aureusVitex negundoHibiscus rosa-sinensisMelaleuca alternifolia.
105,732 views
31,768 downloads

Contributors:

 Sharma Ayushi
,
 Mukati Sandeep
,
 Koshta Ashok
,
 Malviya Sapna
,
 Kharia Anil
Research PaperID: AJPHR1012003

Formulation and Evaluation of Colon Targeted Matrix Tablets of Mesalazine

Jaiswal Anamika, Koshta Ashok, Malviya Sapna, Kharia Anil

ABSTRACTThe present work involves the formulation of colon targeted matrix tablet of Mesalazine by using direct compression method. Excipients including in the formulation are Eudragit S100, Ethyl cellulose, Lactose, Talc, Magnesium stearate. Preformulation studies have also been performed to study the nature of API and compatibility of API with excipients by physical observation and TLC studies. The result showed that API was compatible with all the excipients selected. The tablets were formulated by direct compression method using the selected excipient quantities. The formulated tablets were tested for both pre-compression parameters and post compression parameters as per requirements of standards. Pre-compression parameters such as bulk density, tapped density, compressibility index, Hausner’s ratio and compressibility index. The results obtained indicate that it has good flow property for direct compression. The formulated Mesalazine matrix tablets were coated with enteric polymer Eudragit FS 30D by pan coating method. The prepared tablets were evaluated for weight variation, hardness, thickness, friability, drug content, disintegration time and in-vitro dissolution studies. All these parameters were found to be within the standard limits. Comparative studies of coated Mesalazine tablets and uncoated Mesalazine tablets were evaluated for the hardness, thickness, in-vitro dissolution studies and disintegration time. Out of six formulations, the formulation F6 showed 98.51% drug release at 16 hrs. Since it provide greater protection to the core under acidic condition while at the same time show the fastest drug release under intestinal pH. So the formulation F6 was considered as the confirmatory trial and it was subjected for stability studies up to three months of accelerated stability 400C ± 2C0, 75 % ± 5 % RH and found to be within limits. Keywords: Matrix Tablet, Mesalazine, direct compression method.

Matrix TabletMesalazinedirect compression method.
105,538 views
31,741 downloads

Contributors:

 Jaiswal Anamika
,
 Koshta Ashok
,
 Malviya Sapna
,
 Kharia Anil