Aim:This research aimed to study the potential of PDEN from P. peruviana fruits
(PENC) for regenerating and remodeling HDF.Background:Large wounds are dangerous and require prompt and effective healing. Various efforts
have been undertaken, but have been somewhat ineffective. Plant-derived exosome-like nanoparticles
(PDEN) are easily sampled, relatively cost-effective, exhibit high yields, and are nonimmunogenic.Objective:The objective of the study was to isolate and characterize PDEN from Physalis peruviana
(PENC), and determine PENC’s internalization and toxicity on HDF cells, PENC's ability to regenerate
HDF (proliferation and migration), and PENC ability’s to remodel HDF (collagen I and
MMP-1 production).Methods:PENC was isolated using gradual filtration and centrifugation, followed by sedimentation
using PEG6000. Characterization was done using a particle size analyzer, zeta potential analyzer,
TEM, and BCA assay. Internalization was done using PKH67 staining. Toxicity and proliferation
assays were conducted using MTT assay; meanwhile, migration assay was carried out by employing
the scratch assay. Collagen I production was performed using immunocytochemistry and MMP-1
production was conducted using ELISA.Results:MTT assay showed a PENC concentration of 2.5 until 500 μg/mL and being non-toxic to
cells. PENC has been found to induce cell proliferation in 1, 3, 5, and 7 days. PENC at a concentration
of 2.5, 5, and 7.5 μg/mL, also accelerated HDF migration using the scratch assay in two days.
In remodeling, PENC upregulated collagen-1 expression from day 7 to 14 compared to control.
MMP-1 declined from day 2 to 7 in every PENC concentration and increased on day 14. Overall,
PENC at concentrations of 2.5, 5, and 7.5 μg/mL induced HDF proliferation and migration, upregulated
collagen I production, and decreased MMP-1 levels.Conclusion:Isolated PENC was 190-220 nm in size, circular, covered with membrane, and its zeta
potential was -6.7 mV; it could also be stored at 4°C for up to 2 weeks in aqua bidest. Protein concentration
ranged between 170-1,395 μg/mL. Using PKH67, PENC could enter HDF within 6 hours.
PENC was non-toxic up to a concentration of 500 μg/mL. Using MTT and scratch assay, PENC was
found to elevate HDF proliferation and migration, and reorganize actin. Using immunocytochemistry,
collagen I was upregulated by PENC, whereas MMP-1 concentration was reduced.