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https://doi.org/10.3390/ijms20030541
Title: | Localized delivery of pilocarpine to hypofunctional salivary glands through electrospun nanofiber mats: An ex vivo and in vivo study | Authors: | Muthumariappan S. Ng W.C. Adine C. Ng K.K. Davoodi P. Wang C.-H. Ferreira J.N. |
Keywords: | caspase 3 electrospun nanofiber Ki 67 antigen macrogol nanofiber pilocarpine polyglactin unclassified drug biomaterial nanofiber pilocarpine apoptosis Article biocompatibility biological activity cell proliferation cytotoxicity drug formulation drug release electrospinning encapsulation ex vivo study immunofluorescence in vivo study nonhuman protein degradation protein expression salivary gland scanning electron microscopy xerostomia animal C57BL mouse cell compartmentalization cell death chemistry drug delivery system drug effect female Institute for Cancer Research mouse intradermal drug administration metabolism pathophysiology saliva salivary gland treatment outcome ultrastructure Animals Biocompatible Materials Cell Compartmentation Cell Death Drug Delivery Systems Drug Liberation Female Injections, Intradermal Ki-67 Antigen Mice, Inbred C57BL Mice, Inbred ICR Nanofibers Pilocarpine Saliva Salivary Glands Treatment Outcome |
Issue Date: | 2019 | Citation: | Muthumariappan S., Ng W.C., Adine C., Ng K.K., Davoodi P., Wang C.-H., Ferreira J.N. (2019). Localized delivery of pilocarpine to hypofunctional salivary glands through electrospun nanofiber mats: An ex vivo and in vivo study. International Journal of Molecular Sciences 20 (3) : 541. ScholarBank@NUS Repository. https://doi.org/10.3390/ijms20030541 | Abstract: | Dry mouth or xerostomia is a frequent medical condition among the polymedicated elderly population. Systemic pilocarpine is included in the first line of pharmacological therapies for xerostomia. However, the efficacy of existing pilocarpine formulations is limited due to its adverse side effects and multiple daily dosages. To overcome these drawbacks, a localized formulation of pilocarpine targeting the salivary glands (SG) was developed in the current study. The proposed formulation consisted of pilocarpine-loaded Poly(lactic-co-glycolic acid) (PLGA)/poly(ethylene glycol) (PEG) nanofiber mats via an electrospinning technique. The nanofiber mats were fully characterized for their size, mesh porosity, drug encapsulation efficiency, and in vitro drug release. Mat biocompatibility and efficacy was evaluated in the SG organ ex vivo, and the expression of proliferation and pro-apoptotic markers at the cellular level was determined. In vivo short-term studies were performed to evaluate the saliva secretion after acute SG treatment with pilocarpine-loaded nanofiber mats, and after systemic pilocarpine for comparison purposes. The outcomes demonstrated that the pilocarpine-loaded mats were uniformly distributed (diameter: 384 ± 124 nm) in a highly porous mesh, and possessed a high encapsulation efficiency (~81%). Drug release studies showed an initial pilocarpine release of 26% (4.5 h), followed by a gradual increase (~46%) over 15 d. Pilocarpine-loaded nanofiber mats supported SG growth with negligible cytotoxicity and normal cellular proliferation and homeostasis. Salivary secretion was significantly increased 4.5 h after intradermal SG treatment with drug-loaded nanofibers in vivo. Overall, this study highlights the strengths of PLGA/PEG nanofiber mats for the localized daily delivery of pilocarpine and reveals its potential for future clinical translation in patients with xerostomia. © 2019 by the authors. Licensee MDPI, Basel, Switzerland. | Source Title: | International Journal of Molecular Sciences | URI: | https://scholarbank.nus.edu.sg/handle/10635/174659 | ISSN: | 1661-6596 | DOI: | 10.3390/ijms20030541 |
Appears in Collections: | Elements Staff Publications |
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