Journal
PHARMACEUTICS
Volume 14, Issue 2, Pages -Publisher
MDPI
DOI: 10.3390/pharmaceutics14020358
Keywords
coaxial electrospinning; core-shell nanofibers; buccal delivery; fast-dissolving fibers
Categories
Funding
- National Industrial Development and Logistics Program (NIDLP) [20-0103, 20-0051]
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The electrospun nanofiber system has the potential to improve drug bioavailability and absorption in geriatric patients, especially for drugs with multiple active ingredients. Experimental results showed that the system could effectively prepare and release nifedipine and atorvastatin calcium, indicating potential applications as a buccal drug delivery system.
Geriatric patients are more likely to suffer from multiple chronic diseases that require using several drugs, which are commonly ingested. However, to enhance geriatric patients' convenience, the electrospun nanofiber system was previously proven to be a successful alternative for the existing oral dosage forms, i.e., tablets and capsules. These nanofibers prepared either as single- or multi-layered fibers could hold at least one active compound in each layer. They might also be fabricated as ultra-disintegrated fibrous films for oral cavity administration, i.e., buccal or sublingual, to improve the bioavailability and intake of the administered drugs. Therefore, in this work, a combination of nifedipine and atorvastatin calcium, which are frequently prescribed for hypertension and hyperlipidemia patients, respectively, was prepared in a coaxial electrospinning system for buccal administration. Scanning electron microscopy image showed the successful preparation of smooth, non-beaded, and non-porous surfaces of the drug-loaded nanofibers with an average fiber diameter of 968 +/- 198 nm. In contrast, transmission electron microscopy distinguished the inner and outer layers of those nanofibers. The disintegration of the drug-loaded nanofibers was <= 12 s, allowing the rapid release of nifedipine and atorvastatin calcium to 61% and 47%, respectively, after 10 min, while a complete drug release was achieved after 120 min. In vitro, a drug permeation study using Franz diffusion showed that the permeation of both drugs from the core-shell nanofibers was enhanced significantly (p < 0.05) compared to the drugs in a solution form. In conclusion, the development of drug-loaded nanofibers containing nifedipine and atorvastatin calcium can be a potential buccal delivery system.
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