# Antifungal activity of oily core PEGylated PLGA nanocapsules loaded with Penicillium oxalicum fungal extract: in vitro, in vivo, and in silico study

**Authors:** Engy Elekhnawy, Dalia H. Abdelkader, Duaa Eliwa, Sarah Ibrahim, Moataz A. Shaldam, Walaa A. Negm

PMC · DOI: 10.1186/s12934-025-02891-x · Microbial Cell Factories · 2026-01-16

## TL;DR

This study explores the antifungal potential of nanocapsules loaded with a fungal extract from Penicillium oxalicum, showing effectiveness in lab, animal, and computer models.

## Contribution

The novel use of PEGylated PLGA nanocapsules to deliver antifungal compounds from Penicillium oxalicum extract is introduced.

## Key findings

- PEGylated PLGA nanocapsules showed antifungal activity against Candida albicans with inhibition zones of 10–14 mm.
- In vivo treatment improved organ histology and reduced inflammation markers in infected animals.
- In silico studies confirmed the extract's compounds can inhibit C. albicans aspartic proteinases SAP4-6.

## Abstract

The rise of difficult-to-treat fungal infections necessitates novel therapeutic strategies. In this study, endophytic fungi were isolated from Acalypha hispida leaves and molecularly identified as Penicillium oxalicum via 18S rRNA sequencing. LC–MS/MS analysis of the fungal extract revealed major bioactive compounds, including linoleic acid, sinapinic acid, alternariol monomethyl ether, ellagic acid, and kaurenic acid. Oily-core poly (ethylene glycol) methyl ether-block-poly(lactide-co-glycolide) nanocapsules (PEGylated PLGA NCs) were developed to encapsulate the fungal extract, improving stability and bioavailability. The PEGylated PLGA NCs exhibited controlled particle size, positive surface charge, and spherical morphology. In vitro, the PEGylated PLGA NCs demonstrated antifungal activity against Candida albicans with inhibition zones of 10–14 mm. In vivo, treatment significantly improved histological features of the kidney, liver, and spleen, and reduced tumor necrosis factor-alpha and cyclooxygenase-2 expression. In silico studies further confirmed the potential of the major compounds of the fungal extract to inhibit C. albicans aspartic proteinases SAP4-6. These findings suggest that PEGylated PLGA NCs loaded with P. oxalicum extract represent a promising antifungal therapeutic strategy.

The online version contains supplementary material available at 10.1186/s12934-025-02891-x.

## Linked entities

- **Proteins:** SAP4 (Sap4p), SAP5 (A20/AN1-like zinc finger family protein), SAP6 (aspartyl protease SAP6)
- **Chemicals:** linoleic acid (PubChem CID 5280450), sinapinic acid (PubChem CID 1549091), alternariol monomethyl ether (PubChem CID 5360741), ellagic acid (PubChem CID 5281855), kaurenic acid (PubChem CID 73062)
- **Species:** Penicillium oxalicum (taxon 69781), Candida albicans (taxon 5476), Acalypha hispida (taxon 197604)

## Full-text entities

- **Genes:** COX-2 [NCBI Gene 13080328]
- **Diseases:** vacuolar degeneration (MESH:C536522), necrosis (MESH:D009336), black fungal infection (MESH:D009181), inflammation (MESH:D007249), COVID-19 (MESH:D000086382), cytotoxic (MESH:D064420), bleeding (MESH:D006470), infected (MESH:D007239)
- **Chemicals:** Petroselinic acid (MESH:C008820), flavonoids (MESH:D005419), AME (MESH:C018206), paraffin (MESH:D010232), quinones (MESH:D011809), oleic acid (MESH:D019301), Fluconazole (MESH:D015725), ethyl acetate (MESH:C007650), hematoxylin (MESH:D006416), SA (MESH:C073734), hydrogen (MESH:D006859), oil (MESH:D009821), alkaloids (MESH:D000470), alcohol (MESH:D000438), Water (MESH:D014867), hydrogen peroxide (MESH:D006861), m-PEG-PLGA (MESH:C558447), Tween 80 (MESH:D011136), carbon (MESH:D002244), DCM (MESH:D008752), Pepstatin (MESH:C031375), polymer (MESH:D011108), Span 80 (MESH:C018665), dimethyl sulfoxide (MESH:D004121), ethanol (MESH:D000431), Acetone (MESH:D000096), eosin (MESH:D004801), terpenoids (MESH:D013729), poly(lactide-co-glycolide (MESH:D011098), phenolic acids (MESH:C017616), steroids (MESH:D013256), glycosides (MESH:D006027), H&amp; E (MESH:D006371), Ilicic acid (MESH:C458885), ilicicolin H (MESH:C433880), isocoumarins (MESH:D049934), DMF (MESH:D004126), 8R-HODE (-), Norlichexanthone (MESH:C568539), 7S,8S-DiHODE (MESH:C075808), acetonitrile (MESH:C032159), eudesmane (MESH:C015872), LA (MESH:D019787), iron (MESH:D007501), S (MESH:D013455), lactones (MESH:D007783), carboxylic acid (MESH:D002264), citrate (MESH:D019343), monounsaturated fatty acid (MESH:D005229), amoxicillin (MESH:D000658), PG (MESH:D019946), polyketide (MESH:D061065), PEG-PLGA (MESH:C000589473), formalin (MESH:D005557), EA (MESH:D004610), N (MESH:D009584), ammonium formate (MESH:C030544), xanthone (MESH:C009689), methanol (MESH:D000432), diterpenoid (MESH:D004224)
- **Species:** Symbiodinium sp. Ap5 (species) [taxon 945926], Penicillium (genus) [taxon 5073], Homo sapiens (human, species) [taxon 9606], Penicillium oxalicum (species) [taxon 69781], Candida albicans (species) [taxon 5476], Mus musculus (house mouse, species) [taxon 10090], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Candida [taxon 1535326], Acalypha hispida (chenille plant, species) [taxon 197604]

## Full text

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Source: https://tomesphere.com/paper/PMC12874840