| ORIGINAL ARTICLE |
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| Year : 2018 | Volume
: 3
| Issue : 1 | Page : 8-15 |
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Influence of micronization on the physical properties of salbutamol sulfate as a model drug used in dry powder inhalation
Antesar M Boshhiha1, Nora Anne Urbanetz2
1 Department of Pharmaceutic, Faculty of Pharmacy, University of Benghazi, Benghazi, Libya
2 Faculty of Pharmacy, Institute of Pharmaceutical Technology and Biopharmaceutics, Heinrich Heine University, Dusseldorf, Germany
Correspondence Address:
Dr. Antesar M Boshhiha
Department of Pharmaceutic, Faculty of Pharmacy, University of Benghazi, Alhawari Road 1, Benghazi
Libya
 Source of Support: None, Conflict of Interest: None
DOI: 10.4103/LIUJ.LIUJ_4_18
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Purpose: Investigation of the crystallinity of salbutamol sulfate a model drug used in the dry powder inhalation formulation. Materials and Methods: Salbutamol sulfate was supplied kindly by Lindopharm (Hilden, Germany). Salbutamol sulfate was milled using an air jet milling process, the particle size and morphology were determined using laser diffraction and the scanning electron microscopy. The drug was subjected to conditioning through storage at 52.8% and 75% relative humidity for 24 h, 1 week, and 2 weeks, respectively. The drug crystallinity was investigated using differential scanning calorimetry (DSC), X-ray diffraction, and water vapor sorption techniques. Results and Discussion: Conditioning of salbutamol sulfate after micronization lowers the glass transition (Tg) temperature of the amorphous parts present at particle surface, which enhances particle mobility for more rearrangement associated with water expelling. This transformation may result in deviation from the original particle size obtained after milling out of respirable range. DSC and X-ray diffraction show no detectable amorphous drug since no detectable Tg observed. Alternatively, water vapor sorption shows a small amount of amorphous salbutamol sulfate at the particle surface, which recrystallizes at 52.8% relative humidity after approximately 2 weeks of conditioning. Conclusion: The amorphous regions can be generated in crystalline materials during processing. The level of amorphous materials can affect every step of pharmaceutical formulation, storage, and stability. However, quantification of low levels of amorphous content still poses considerable challenge. This study confirms that, the water vapor sorption technique is useful in the quantification of a small amount of drug amorphous content.
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