Microwave non-destructive testing technique for characterization of HPMC-PEG 3000 films - PowerPoint PPT Presentation

1 / 18
About This Presentation
Title:

Microwave non-destructive testing technique for characterization of HPMC-PEG 3000 films

Description:

Microwave 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 ... – PowerPoint PPT presentation

Number of Views:385
Avg rating:3.0/5.0
Slides: 19
Provided by: NORKH
Category:

less

Transcript and Presenter's Notes

Title: Microwave non-destructive testing technique for characterization of HPMC-PEG 3000 films


1
Microwave 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

2
CONTENT
  • 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

3
1.0 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.

6
2.0 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.

8
Sample 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.
10
3.0 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.
11
ii) DSC analysis
12
iii) FTIR analysis
13
iv) 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.

15
4.0 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.

16
ACKNOWLEDGEMENT
  • 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.

17
REFERENCES
  • 1 S.T. Narisetty and P. Ramesh, Transdermal
    Delivery of Zidovudine Effect of Vehicles on
    Permeation Across Rat Skin and their Mechanism of
    Action, Euro. J. Pharm. Sc., vol. 18, pp. 71-79,
    2003.
  • 2 N.K. Pramila and R.V. Pradeep, Eudragits
    Role as Crystallization Inhibitors in
    Drug-In-Adhesive Transdermal Systems of
    Estradiol, Euro. J. Pharm. and Biopharm., vol.
    52, pp. 173180, 2001.
  • 3 K.J. Amit, S.T. Narisetty and P. Ramesh,
    Transdermal Drug Delivery of Imipramine
    Hydrochloride. I. Effect of Terpenes, J. Cont.
    Rel., vol. 79, pp. 93101, 2002.
  • 4 X. Yu, X. Bai and G. Yunhua, Controlled
    Transdermal Delivery of Model Drug Compounds by
    MEMS Microneedle Array, Nanomedicine
    Nanotechnology, Biology, and Medicine, vol. 1,
    pp. 184-190, 2005.
  • 5 C.W. Robert, J.A. Melvin and H.B. William,
    CRC Handbook of Chemistry and Physics, 69th Ed.,
    CRC Press, Inc., Florida, 1989.
  • 6 A. Zulkifly, D.P. Roger and W.K. Robert,
    Determination of the Dielectric Constant of
    Materials from Effective Refractive Index
    Measurements, IEEE Trans. on Inst. Meas., vol.
    47, pp. 148-152, 1998.
  • 7 A. Nor Khaizan, T.W. Wong, D.K. Ghodgaonkar
    and T. Mohd Nasir, Characterization of
    Hydroxypropylmethylcellulose Films using
    Microwave Non-Destructive Testing Technique,
    Journal of Pharmaceutical and Biomedical
    Analysis, vol. 43, pp. 549557, 2007.

18
THANK YOU
Write a Comment
User Comments (0)
About PowerShow.com