4.8 Article

Atomic Layer Deposition Coating on the Surface of Active Pharmaceutical Ingredients to Reduce Surface Charge Build-Up

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 14, 期 23, 页码 27195-27202

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.2c05761

关键词

atomic layer deposition (ALD); palbociclib; pazopanib HCl; ? potential; surface morphology

资金

  1. Department of Biotechnology, Ministry of Science and Technology [BT/COE/34/SP15097/2015]
  2. Council of Industrial and Scientific Research [09/086(1366)2019-EMR-1]

向作者/读者索取更多资源

This study demonstrates the use of atomic layer deposition (ALD) to uniformly coat drug particles, reducing surface charge and improving the properties of the particles. The coated drugs showed similar thermal stability, delayed dissolution rate, and no statistically significant cytotoxicity compared to the uncoated samples.
consist of solid therapeutic particles that may acquire electrostatic charge during milling and grinding operations. This may result in the agglomeration of particles, thereby reducing the flowability and affecting the homogeneity of the drug formulation. Electrostatic charge build-up may also lead to fire explosions. To avoid charge build-up, APIs are often coated with polymers. In this paper, atomic layer deposition (ALD) using metal oxides such as Al2O3 and TiO2 on APIs, namely, palbociclib and pazopanib HCl, has been utilized to demonstrate a uniform coating that results in a significant reduction in the surface charge of the drug particles. Kelvin probe force microscopy (KPFM) shows a 4-fold decrease in the surface contact potential of uncoated pazopanib HCl (2.3 V) to 0.52 and 0.82 V in TiO2-and Al2O3-coated APIs, respectively. Also, the ?? potential indicated a 4-fold decrease in the surface charge on coating pazopanib HCl, i.e., from ???32.9 mV to ???7.51 and ???8.51 mV in Al2O3 and TiO2, respectively. Surface morphology, thermal stability, dissolution studies, and cytotoxicity of the drug particles after coating were also examined. Thermal analysis indicated no change in the melting temperature (Tm) after coating. ALD coating was found to be uniform and conformal as observed in images obtained from scanning electron microscopy (SEM) and scanning electron microscopy???energy-dispersive X-ray spectroscopy (SEM???EDS). The rate of dissolution was found to be delayed by the coating, and thus ALD offers slower drug release. Coating APIs with TiO2 and Al2O3 did not induce statistically significant cytotoxicity compared to the uncoated samples. The results presented in this study demonstrate that ALD coating can be used to reduce surface charge build-up and enhance the bulk properties of the drug particles without affecting their physicochemical properties.

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