Title: Microwave non-destructive testing technique for characterization of HPMC-PEG 3000 films
1Microwave non-destructive testing technique for
characterization of HPMC-PEG 3000 films
- Nor Khaizan Anuar1,3, Wong Tin Wui1,3, Mohd
Nasir Taib2,3 and Deepak K. Ghodgaonkar4 - 1Particle Design Research Group, Faculty of
Pharmacy, Universiti Teknologi MARA, 40450, Shah
Alam, Selangor, Malaysia - 2Faculty of Electrical Engineering, Universiti
Teknologi MARA, 40450, Shah Alam, Selangor,
Malaysia - 3Non-Destructive Biomedical and Pharmaceutical
Research Centre, Universiti Teknologi MARA,
40450, Shah Alam, Selangor, Malaysia - 4Dhirubhai Ambani Institute of Information and
Communication Technology, DA-IICT Near Indroda
Circle, Gandhinagar, 382007, Gujarat, India - wongtinwui_at_salam.uitm.edu.my
2CONTENT
- 1.0 INTRODUCTION
- 2.0 EXPERIMENTAL
- 2.1 Materials
- 2.2 Sample preparation
- 2.3 Physicochemical characterization
- 3.0 RESULTS AND DISCUSSION
- 4.0 CONCLUSION
- ACKNOWLEDGEMENT
- REFERENCES
31.0 INTRODUCTION
- Transdermal drug delivery system (TDDS) utilizes
the skin for the delivery of drug molecules from
the surface of the skin, through its layers, to
the circulatory system. - Quality control of matrix characteristics, such
as state of polymer-polymer and drug-polymer
interaction, is essential with respect to the
therapeutic effectiveness of a TDDS.
4- In the pharmaceutical industry, the analytical
techniques such as differential scanning
calorimetry (DSC) and Fourier transform infra-red
spectroscopy (FTIR) have long been employed to
determine the matrix characteristics of a TDDS. - However, these techniques result in sample being
unrecoverable from test and restrict the analysis
to statistically selected samples.
5- The present study sets to explore the
applicability of microwave NDT technique as an
optional tool to characterize the matrix property
of polymer film for use as a transdermal drug
delivery system.
62.0 EXPERIMENTAL
- 2.1 Materials
- Hydroxypropylmethylcellulose (HPMC, Dow Chemical
Company, USA) matrix polymer. - Loratadine (Morepen Laboratories, India) model
drug. - Polyethylene glycol (PEG 3000, Merck, Germany)
plasticizer.
7- 2.2 Sample preparation
- The films were prepared using solvent evaporation
method. - The films were conditioned in a desiccator at 25
? 1 C and at three different levels of relative
humidity (25 ? 5 , 50 ? 5 and 75 ? 5 ) for at
least 5 days prior to the physicochemical
characterization.
8Sample HPMC (mg) PEG 3000 (mg) Loratadine (mg)
H0 37.5 0 0
P0 37.5 3.75 0
P1 37.5 3.75 5
P2 37.5 3.75 20
Table 1 Theoretical contents of HPMC, PEG 3000
and loratadine in films.
9- 2.3 Physicochemical characterization
- The formed film was subjected to drug content
assay using UV spectrophotometry technique, DSC,
FTIR and microwave NDT analysis.
Fig. 1 Rectangular dielectric waveguide (RDWG)
measurement system.
103.0 RESULTS AND DISCUSSION
i) Drug content analysis
Sample Film thickness (mm) Relative humidity () Relative humidity () Relative humidity ()
Sample Film thickness (mm) 25 50 75
Sample Film thickness (mm) Loratadine content (w/w) Loratadine content (w/w) Loratadine content (w/w)
H0 0.031 ? 0.006 0 0 0
P0 0.036 ? 0.003 0 0 0
P1 0.064 ? 0.015 12.15 ? 0.32 13.59 ? 0.36 13.06 ? 0.16
P2 0.114 ? 0.033 39.06 ? 0.93 35.06 ? 1.14 38.04 ? 1.34
Table 2 Drug content of films measured using the
UV spectrophotometry technique.
The drug content of films was not affected by the
level of relative humidity in the storage chamber
(ANOVA p gt 0.05).
A flat film was formed.
A thicker film was formed in sample containing a
higher content of drug load.
11ii) DSC analysis
12iii) FTIR analysis
13iv) Microwave NDT analysis
14- From the previous study of our laboratory, it was
found that the measurement of microwave NDT test
at 8 GHz was sensitive to the chemical
environment involving polar moiety such as O-H
functional group, while it was greatly governed
by the less polar C-H moiety in test conducted at
12 GHz. - The present findings indicated that the changes
of both polar and apolar environments of HPMC-PEG
3000 films were reflected accordingly by the
microwave NDT measurements conducted at the
frequency bands of 8 and 12 GHz respectively.
154.0 CONCLUSION
- The measurements of microwave NDT test at 8 and
12 GHz were sensitive to the changes of chemical
environment in matrix involving polar functional
group such as O-H moiety and less polar
functional group such as C-H and aromatic CC
moieties. - The present investigation verified that the
microwave NDT technique has the capacity to
evaluate the state of interaction between
polymer, plasticizer and/or drug of a binary
polymeric matrix, in addition to the existing DSC
and FTIR techniques.
16ACKNOWLEDGEMENT
- The authors wish to express their heart-felt
gratitude to Institute of Research, Development
and Commercialization, UiTM for financial support
and motivation given throughout the research
project.
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18THANK YOU