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Thermal Analysis Methods in Pharmaceutical Quality Control
ISSN: 2329-9053
Journal of Molecular Pharmaceutics & Organic Process Research
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  • Editorial   
  • J Mol Pharm Org Process Res 2015, Vol 3(1): e121
  • DOI: 10.4172/2329-9053.1000e121

Thermal Analysis Methods in Pharmaceutical Quality Control

Monajjemzadeh F,1,2* and Ghaderi F3
1Department of Pharmaceutical and Food Control, Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran
2Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
3Student research committee of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran
*Corresponding Author: Monajjemzadeh F,, Associate Professor, Department of Pharmaceutical and Food Control, Tabriz University of Medical Sciences, Tabriz, Zip Code: 5166414766, Iran, Tel: +9841133392606, Fax: +9841133344798, Email: Monaggemzadeh@tbzmed.ac.ir

Received: 19-Feb-2015 / Accepted Date: 20-Feb-2015 / Published Date: 25-Feb-2015 DOI: 10.4172/2329-9053.1000e121

Thermal analysis is defined as a group of physical-chemical methods which the properties of studied material are measured as a function of temperature or time while the sample is placed under a controlled temperature program. The program may include heating or cooling (dynamic), or fixed temperature (isothermal), or a combination of these methods [1,2]. Different multi-component techniques including thermogravimetry, differential thermal analysis, differential scanning calorimetry and thermo-microscopy are available instrumentally. Nowadays, these methods has gained significant attention in both quality control and functional research on Industries such as polymers, pharmaceuticals, metals and alloys [3,4]. Thermogravimetry (TG) or Thermogravimetric analysis (TGA) is a fundamental laboratory instruments applied for investigation of the material properties in various fields such as pharmaceutical, environmental, food and petrochemical applications [5]. TGA is a technique in which the amount of weight change of a substance, is monitored either as a function of controlled temperature, or isothermally as a function of time, in an atmosphere of N2, He, air, other gas, or in vacuum [6]. The differential thermal analysis (DTA) is common thermal analysis method in which an analyte and an inert reference are heating at a certain heating rate while any temperature change is recorded. DTA is a popular tool used to characterize pharmaceuticals, foods, biologicals, organic and inorganic chemicals and briefly applied to measure endothermic and exothermic transitions as a function of temperature [7,8]. Differential scanning calorimetry or DSC is a popular thermoanalytical technique ranging from the pharmaceutical science to applied research. DSC monitors the difference in the amount of required heat to increase the temperature of a sample and reference (which should have an acceptable heat capacity in the range of scanned temperatures) as a function of temperature [9,10].

Thermo microscope or hot stage microscope (HSM) is a microscope coupled with a hot stage accessory with excellent heating and cooling systems ranging from -200°C to 500°C. For study the visual changes a color camera is connected to the microscope. This method records the surface temperature and thermal conductivity of an interface [11-13].

In pharmaceutical control all mentioned thermal techniques are of significant importance. The drug substance purity, polymorphism, stability can be easily evaluated using thermal analysis [10,14-17]. In the case of pharmaceutical excipients, the purity, glass transition temperature of polymeric materials and drug-excipient compatibility is simply monitored using these methods [18,19]. Recently kinetic analysis has been performed based on different thermal techniques such as DSC and TGA, and various models have been proposed in order to analyze the Arrhenius kinetic parameters [20-22].

References

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  2. Haines PJ (1995) Thermal methods of analysis: principles, applications and problems: Chapman & Hall.
  3. Giron D (1995) Thermal analysis and calorimetric methods in the characterisation of polymorphs and solvates. Thermochimicaacta 248: 1-59.
  4. Haines PJ (2002) Principles of thermal analysis and calorimetry: Royal society of chemistry.
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  10. Monajjemzadeh F, Hassanzadeh D, Valizadeh H, Siahi-Shadbad MR, Mojarrad JS, et al. (2009) Compatibility studies of acyclovir and lactose in physical mixtures and commercial tablets. European Journal of Pharmaceutics and Biopharmaceutics 73: 404-413.
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  12. Chadha R, Arora P, Bhandari S, Bala M (2012) Thermomicroscopy and its pharmaceuticals applications. Current Microscopy Contributions to Advances in Science and Technology 2: 1013-1024.
  13. Monajjemzadeh F, Farjami A (2014) Common Problems in Stress Testing of Pharmaceutical Preparations. J Mol Pharm Org Process Res 2: e117.
  14. Monajjemzadeh F, Hamishehkar H, Zakeri-Milani P, Farjami A, Valizadeh H (2013) Design and Optimization of Sustained-Release Divalproex Sodium Tablets with Response Surface Methodology. AAPS Pharm Sci Tech 14: 245-253.
  15. Hamishehkar H, Valizadeh H, Alasty P, Monajjemzadeh F (2014) Spray Drying as a Fast and Simple Technique for the Preparation of Extended Release Dipyridamole (DYP) Microparticles in a Fixed Dose Combination (FDC) Product with Aspirin. Drug research 64: 104-112.
  16. Monajjemzadeh F, Ebrahimi F, Zakeri-Milani P, Valizadeh H (2014) Effects of Formulation Variables and Storage Conditions on Light Protected Vitamin B12 Mixed Parenteral Formulations. Advpharma bulletin 4: 329.
  17. Monajjemzadeh F (2014) LC-Mass as a Complementary Method in Detecting Drug-Excipient Incompatibility in Pharmaceutical Products. J Mol Pharm Org Process Res 2: e110.
  18. de Barros, Lima Í P, Oliveira TS, MendonçaCMS, Euzébio G, et al. (2014) Compatibility study between hydroquinone and the excipients used in semi-solid pharmaceutical forms by thermal and non-thermal techniques. Journal of Thermal Analysis and Calorimetry: 1-14.
  19. deMendonça CMS, de Barros Lima IP, Soares Aragão CF, Barreto Gomes AP (2014) Thermal compatibility between hydroquinone and retinoic acid in pharmaceutical formulations Journal of Thermal Analysis and Calorimetry 115: 2277-2285.
  20. Bianchi O, Fioriob R, De Martinsb JN, Zatterab AJ, Cantoc LB, et al. (2008) Assessment of Avrami, Ozawa and Avrami–Ozawa equations for determination of EVA crosslinking kinetics from DSC measurements. Polymer Testing 27: 722-729.
  21. Ozawa T (2000) Thermal analysis—review and prospect. Thermochimica Acta 355: 35-42.
  22. Ozawa T (1971) Kinetics of non-isothermal crystallization. Polymer 12: 150-158.

Citation: Monajjemzadeh F, Ghaderi F (2015) Thermal Analysis Methods in Pharmaceutical Quality Control. J Mol Pharm Org Process Res 3: e121. Doi: 10.4172/2329-9053.1000e121

Copyright: ©2015 Monajjemzadeh F, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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