Trends in drug delivery (vol1, issue2)

Page 1

Trends in

Drug Delivery (TDD) May - August 2014

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Dr. A.J. Vanisree Assistant Professor, Department of Biochemistry University of Madras, Chennai, India.

Dr. Abhay Dharamsi Prof. & Head, Dept. of Pharmaceutics, Maliba Pharmacy College, Gujarat, India.

Dr. Anil Bansal Chairman, Department of Pharmacology, J. N. Medical College, AMU, Aligarh, India.

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Dr. Bhavin Marolia Assistant Prof., Dept. of Quality Assurance & Pharmaceutical Analysis, Maliba Pharmacy College, Bardoli, India.

Divya Suares Assistant Professor, NMIMS University, India.

Gautam Singhvi Department of Pharmacy, BITS, Pilani, India.

Dr. Jayarajakumar Kalaimani Faculty of Pharmacy, AIMST University, Bedong, Malaysia

Dr. Kashmira Gohil Professor and HOD, Shree Dhanvantari Pharmacy College, Gujarat, India.

Dr. Koteshwara K.B Professor Dept. of Pharmaceutics, Manipal College of Pharmaceutical Sciences, Manipal University, India

Dr. Mahalaxmi Rathnanand Associate Prof., Dept. of Pharmaceutics Manipal College of Pharmaceutical Sciences, Manipal, India.

Dr. Mayur Patel Associate Professor, Dept. of Pharmaceutical Science, Institute of Pharmacy, Nirma University, Ahmedabad, Gujarat, India.


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Dr. Nayana Associate Professor, Pharmacology, J N Medical College, Belgaum, India.

Dr. Pranav Shah Associate Professor, Maliba Pharmacy College, Surat, Gujarat, India.

Dr. Rafik Karaman Faculty of Pharmacy Al-Quds University, Jerusalem.

Dr. S. K. M. Habeeb Assistant Prof., Dept. of Bioinformatics, School of Bioengineering, SRM University, India.

Dr. S. Shanmugam Prof. & Head, Dept. of Pharmaceutics, Adhiparasakthi College of Pharmacy, T.N, India.

Dr. Shashank K Singh Senior Scientist, CSIR-Indian institute of Integrative Medicine , Canal Road Jammu, India

Soh Yee Chang Lecturer, Faculty of Pharmacy, UiTM Puncak Alam Campus, Malaysia.

Sonia Pandey Assistant Professor, Maliba Pharmacy College Uka Tarsadia University, Surat, Gujrat, India.

Dr. Srinivas Mutalik Associate Professor, Department of Pharmaceutics, Manipal University, India.

Dr. Tripura Sundari Assistant Professor, SPPSPTM, NMIS, Mumbai, India.

Dr. V. Ravichandran Faculty of Pharmacy, AIMST University, Semeling ,Kedah, Malaysia.

Dr. Viral Dineshchandra Jagiwala Assistant Professor, Shree Dhanvantary Pharmacy College, Gujarat, India.


Editorial Board

Dr. Ganga Srinivasan

Dr. Vivek Bhosale

Professor in Pharmaceutics at VES College of Pharmacy, Mumbai, India.

Scientist, Division of Clinical and Experimental Medicine CSIR-Central Drug Research Institute, India.

Dr. Yahaya Bin Hassan

Dr. Santanu Chakraborty

Head, Faculty of Pharmacy, Universiti Teknologi MARA(UiTM) Malaysia.

Assistant Professor, Department: Pharmaceutics, Dr. B. C. Roy Engineering College, Kolkata, India.

Dr. Sandip Prabhakar Zine

Dr. Nahlah Elkudsiah Ismail

Assistant Professor, Department of Pharmaceutical Chemistry,Vivekanand Education Society's College of Pharmacy, Mumbai, India.

Faculty of Pharmacy, Universiti Teknologi MARA (UiTM) Puncak Alam Campus, Bandar Puncak Alam, Selangor, Malaysia.

Dr. Mudit Dixit Assistant Professor, (Pharmaceutics) (Senior Grade), NGSM Instituteof Pharmaceutical Sciences, Mangalore, India.


Director's Desk

STM JOURNALS

I take the privilege to present the print version for the Volume 1 Issue (2) of Trends in Drug Delivery. The intension of TDD is to create an atmosphere that stimulates creativeness, research and growth in the area Drug Delivery. The development and growth of the mankind is the consequence of brilliant Research done by eminent Scientists and Engineers in every field. TDD provides an outlet for Research findings and reviews in areas of Drug Delivery found to be relevant for National and International recent developments & research initiative. The aim and scope of the Journal is to provide an academic medium and an important reference for the advancement and dissemination of Research results that support high level learning, teaching and research in the domain of Drug Delivery. Finally, and Authors for their continued support and invaluable contributions and suggestions in the form of authoring I express my sincere gratitude and thanks to our Editorial/ Reviewer board write ups/ reviewing and providing constructive comments for the advancement of the journals. With regards to their due continuous support and co-operation, we have been able to publish quality Research/Reviews findings for our customers base. I hope you will enjoy reading this issue and we welcome your feedback on any aspect of the Journal.

Dr. Archana Mehrotra Director STM Journals


Trends in Drug Delivery

Contents

1. Synthesis and Electrochemical Study of 1-[2', 4'-dinitrophenyl)-3, 5-dimethyl-4[4''-(substituted)sulphonamoylphenyl] Azopyrazoles Shrinarayan Karaiya, Ritesh Mishra, Ramji Lal Yadav, Virendra K. Arya, Hitesh Malvia

1

2. Formulation and Evaluation of Transdermal Drug Delivery of Piroxicam Mudit Dixit, P. K. Kulkarni, R Narayana Charyulu

8

3. Regenerative Endodontics: Nano 3D scaffolds as Dental Materials and Stem Cells for Dental Tissue Regeneration Rachna Dhani, Shashank K Singh

14

4. Intrapocket Drug Delivery System: A Spatial Tool for Periodontitis Jain J., Srinivasan G.

24


Trends in Drug Delivery Volume 1, Issue 2 www.stmjournals.com

Synthesis and Electrochemical Study of 1-[2′, 4′-dinitrophenyl)-3, 5-dimethyl-4[4′′-(substituted)sulphonamoylphenyl] Azopyrazoles Shrinarayan Karaiya1*, Ritesh Mishra2, Ramji Lal Yadav1, Virendra K. Arya1, Hitesh Malvia3 1

School of Studies in Chemistry, Jiwaji University, Gwalior, India Analytical Research & Development Department, Medilux Laboratories Pvt. Ltd. Pithampur, Dist. Dhar, India 3 School of Chemical Sciences, DAVV, Indore, India

2

Abstract Electrochemical behavior of 1-(2',4'-dinitrophenyl)-3,5-dimethyl-4-[4"-(substituted) sulphonamoylphenyl] azopyrazole (DDSPA) was studied in Britton-Robinson (BR) buffer range of pH 3.5–12 at dropping mercury electrode (DME) and glassy carbon electrode (GCE). Cathodic differential pulse polarographic peak is obtained at DME in the pH range 3.5–12. Cyclic voltammogram exhibited a well-defined, irreversible cathodic and anodic peak at GCE. At pH 3.5–12, the reduction peak exhibited a tendency to split into two peaks. The first 8e- peak has been assigned to the reduction of two nitro groups to hydroxylamine group and second 2e- peak has been assigned to the reduction of azo group to hydrazono group (–NH–NH–). A product of controlled potential electrolysis (CPE) was characterized by elemental and spectral analysis.

Keywords: azopyrazoles, polarography, voltammetry, CPE, electrochemistry

TDD (2014)© STM Journals 2014. All Rights Reserved


Trends in Drug Delivery Volume 1, Issue 2 www.stmjournals.com

Formulation and Evaluation of Transdermal Drug Delivery of Piroxicam Mudit Dixit1*, P. K. Kulkarni2, R Narayana Charyulu1 1

Department of Pharmaceutics, NGSM Institute of Pharmaceutical sciences, Nitte University, Mangalore, Karnataka, India 2 Department of Pharmaceutics, J.S.S College of pharmacy, J.S.S University, Mysore, India

Abstract The aim of the present study was to formulate transdermal films loaded with Piroxicam (PX). Transdermal films were prepared by using sodium alginate (SA) and xanthan gum (XG) as biopolymers by varying the blend ratios viz., 10:0, 8:2, 6:4, 4:6 and 2:8 (w/w %) through solution casting method. The drug loaded membranes were evaluated for thickness, tensile behaviours, and content uniformity. In-vitro diffusion was determined by Franz diffusion cell. Piroxicam was found to be compatible and stable with the prepared formulation as confirmed by Fourier transform infrared spectroscopy (FTIR) and Differential Scanning Calorimetry (DSC), studies. Invitro release studies revels effectiveness after 24 h. The study results suggest that biopolymer based Transdermal films are potential vehicles for improved transdermal delivery of PX for effective therapy.

Keywords: Piroxicam, Sodium alginate, Xanthan gum, Transdermal release, Skin permeation

TDD (2014)Š STM Journals 2014. All Rights Reserved


Trends in Drug Delivery Volume 1, Issue 2 www.stmjournals.com

Regenerative Endodontics: Nano 3D scaffolds as Dental Materials and Stem Cells for Dental Tissue Regeneration Rachna Dhani1, Shashank K Singh2* 1

Department of Conservative Dentistry & Endodontics Indira Gandhi Government Dental College and Hospital, Jammu, India 2 Cancer Pharmacology Division, CSIR-Indian Institute of Integrative Medicine Canal road, Jammu, India

Abstract In dentistry, for maintaining any tissue in a healthy state, focus is on prevention, treatment and repair of the diseased tissue. Current treatments for diseases of tooth structures rely on the use of classical endodontic procedures which in some cases are limited success rate. The use of stem cells in regenerative therapies have been shown to have promising applications in various debilitating diseases like neurodegenerative disease, diabetes, cancer and dental diseases etc. Regenerative dentistry is addressing various complications involves the in vitro creation of cells/tissues for replacement therapy that stimulate the body’s own regenerative capabilities. Regenerative dentistry represents an attractive multidisciplinary therapeutic approach that combines traditional restorative/surgery techniques and benefits from recent advances in stem cell biology, genomics, proteomics and material sciences. Dental Pulp Stem Cells or (DPSCs) are well characterized multipotent stem cells that have the potential to differentiate into a variety of cell types used for regenerating the tooth. Regenerating and reengineering the decayed pulp structure requires the design of scaffolding materials that mimic the architecture of a natural dental extracellular matrix (ECM) and provide suitable environments for the attachment, proliferation, differentiation, and biomineralization of dental pulp stem cells (DPSCs) to grow. Three-dimensional (3D) biocompatible hybrid scaffolds mimic the nano-structured architecture and chemical composition of a natural dental ECM. DPSCs had a significantly higher proliferation rate on 3D hybrid scaffolds. Hybrid scaffolds significantly promote the differentiation and bio mineralization of the human DPSCs. In summary, using the Hybrid Nano 3D scaffolds which provides an excellent environment for the growth and differentiation of human DPSCs and are promising treatment modality in endodontic procedures for dentin/pulp tissue regeneration and restoration of natural tooth.

Keywords: Embryonic Stem Cells (ESC), pluripotent stem (iPS), Dental Pulp Stem Cells, or (DPSCs), (3D) scaffolds

TDD (2014)Š STM Journals 2014. All Rights Reserved


Trends in Drug Delivery Volume 1, Issue 2 www.stmjournals.com

Intrapocket Drug Delivery System: A Spatial Tool for Periodontitis Jain J., Srinivasan G.* VES College of Pharmacy, Chembur, Mumbai, India Abstract Periodontitis is a disease attributable to multiple infectious agents. It results from extension of the inflammatory process initiated in the gingiva to the supporting periodontal tissues. Periodontal pockets provide natural reservoir bathed by gingival crevicular fluid that is easily accessible for the insertion of a delivery device. Intrapocket, sustained release systems have emerged as a novel paradigm for the future research. Controlled release delivery of antimicrobials is a therapeutic intervention directly into periodontal pockets and is available in various forms like gels, monolithic devices, irrigation systems, chips, films, strips, microspheres, fibers, etc. It is an effective monotherapy that has evoked a great interest and appears to hold a sound promising result in periodontal treatment these local agents bypass the adverse effects of systemically administered antimicrobial agents, as well stabilize the attachment apparatus and reduce the probing depth thereby allowing better control and management of periodontal disease.

Keywords: gingivitis, periodontitis, local drug delivery, periodontal pocket

TDD (2014)Š STM Journals 2014. All Rights Reserved


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