Please use this identifier to cite or link to this item: 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
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