DEVELOPMENT OF BIO COMPATIBLE NANO PARTICLES OF VARIOUS DRUGS
AND THEIR POTENTIAL OUTCOMES IN FIELD OF PHARMACEUTICAL
NANOTECHNOLOGY
INTRODUCTION
Swift advancement in fabrication of nanoparticles having identical size, composition and shape
have started uprising in the field of pharmaceutical sciences. From the last decade, development
of nano size based drug delivery systems has attracted augmented attention of researchers. In fast-
developing field of nanotechnology nano size based drug delivery systems are leading due to
numerous potential uses in pharmaceutical drug delivery and other fields of sciences. Because of
unique size dependent properties, these drug delivery systems offers the opportunity to develop
novel ways for treating diseases. The assimilation of drugs into nano carrier systems gives a new
archetype in drugs delivery, used for drug targeting at secondary and tertiary levels. These drug
delivery systems as oral dosage form, potentially enhance the lymphatic transport, thus reducing
hepatic first pass metabolism and boosted oral bioavailability.
ABOUT PROJECT
In this project efforts will be made for Selection of excipients/carrier systems including lipids,
surfactants and co-surfactants, Adaptation of nanotechnology based approaches to enhance
solubility of different drugs, assessment of different approaches developed for the solubility
enhancement , dissolution followed by intestinal permeability for drugs and some other parameters
such as compatibility studies, spectral analysis and stability studies by using different techniques
like Zeta Sizer, Scanning Electron Microscopy(SEM), Transmission Electron Microscopy (TEM),
Differential Scanning Calorimetry (DSC), Fourier Transform Infra-Red (FTIR), X-Ray
Diffraction (XRD), Atomic Force Microscopy (AFM) etc followed by dosage form designing,
Evaluation of approaches for extent of upgrading of these parameters , assessment of suitable
approach for increase in oral bioavailability, in vivo evaluation such as pharmacokinetic,
pharmacodynamic and toxicological studies using different animal models.
COMPARISON WITH CONVENTIONAL TECHNOLOGY
Conventional formulation strategies may no longer be enough for poorly aqueous soluble drugs
emerged from drug discovery. In recent pharmaceutics, sophisticated drug delivery approaches
such as nano size based drug delivery systems become a vital technology in the development of
new drug entities. In addition to improving solubility and bioavailability, these drug delivery
systems also offer many other clinical advantages over conventional formulations for many poorly
soluble compounds, including:
a. Uniform dosing regimen
b. Reduce therapeutic dose as a result of better drug absorption
c. Decrease hepatic metabolism of drugs because of probable lymphatic transport of
compounds
d. Elimination or decrease of food effects on bioavailability of a compound hence improve
dose flexibility
e. Elimination or decrease of inter- and intra- subject variability because of reduced effects
of GIT variability on solubilization.
Nano drug delivery is also a smart option for controlled drug release and targeted drug delivery.
Using molecular assembly and coating technologies, formulations can be designed to tailor a
desired release profile and target it to a specific site.
GANTT CHART OF THE STUDY
Activity
Activities
Number 1st Quarter 2nd Quarter 3rd Quarter 4th Quarter
1. Literature study and Pre-
formulation study of raw
material
2. Preparation of
Nanoparticles by using
different techniques
Characterization of
Nanoparticles by
SEM/TEM/Zeta sizer
etc
Characterization of
3.
nanoparticles by AFM,
DSC, FTIR, XRD etc
Dosage form designing
In- Vitro Study
In- Vivo Study
4.
Documentation and
Publication
RESEARCH OUTCOMES
Proposed study is highly related with emerging area of nanotechnology which is a
multidisciplinary field with great scope and immense potential in numerous areas such as
pharmaceutical science, materials science, physics, chemistry, environmental sciences, materials
engineering, agriculture, food science, etc. Our research deals with the preparation of nano size
based drug delivery systems by cost effective methods for drugs having low bioavailability which
will be incorporated in these drug delivery systems.
Proposed work will show its impacts in the following ways:
TO ME AND MY UNIVERSITY
Advance my education through various learning opportunities, both formally and through
projects and research activities, which will be determined in collaboration with Prof. Zihei
Dai (supervisor), University of Peking and China our friend country.
Develop my skills by participating in other research projects of my supervisor
Publish many original research results obtained during my tenure in appropriate journals
and other recognized media; and
Attend scientific conferences agreed between me and my supervisor to present our results
(subject to the availability of travel funds).
NATIONAL & SCIENTIFIC OUTCOMES
Current proposal will also prove quite effective in strengthening our institutional facilities on
synthesis of nanostructured materials, characterization and their applications in the
pharmaceutical sciences. Moreover, our experimental data resulting from the proposed
research will be of great worth which can be shared at national/international scientific forum
for reflection of our quality research. From this project, it is expected that at least two
presentations at national and international level would be generated. Dissemination of the
acquired data in internationally reputed journals of impact factor is an integral part of our
scientific data sharing plan. We expect that more than three research articles can be generated
from this proposed work.
Positive opinion will be established about pharmaceutical industries by giving them new
methods for the development of cost-effective drug delivery system. It will help in
improving patient compliance rate.
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