# Development of bioengineered SPIONs using Carica monoica extract: evaluation of antioxidant and anticancer activity of human cervical cancer cells (SiHa)

**Authors:** Xiyi Tian, Haiyuan Yang

PMC · DOI: 10.1515/biol-2025-1258 · Open Life Sciences · 2026-02-12

## TL;DR

This paper describes a new method to create sustainable nanoparticles using Carica monoica extract, which show strong antioxidant and anticancer effects on cervical cancer cells.

## Contribution

The study introduces a novel green synthesis method using Carica monoica extract to create SPIONs with dual antioxidant and anticancer properties.

## Key findings

- CM-SPIONs showed significant, dose-dependent antioxidant activity.
- The nanoparticles exhibited potent cytotoxicity against SiHa cervical cancer cells with an IC50 of 22 ± 0.7 μg/ml.
- Cell death was confirmed to be primarily through apoptosis.

## Abstract

This study pioneers the green synthesis of SPIONs using a novel bioresource: Carica monoica leaf extract as a reducing and capping agent. This method not only emphasizes sustainability but also uniquely leverages the specific phytochemical profile of C. monoica to create a synergistic therapeutic platform. Comprehensive characterization using UV-vis, XRD, TEM, EDX, and FTIR, Zeta potential and VSM confirmed the successful creation of hexagonal, superparamagnetic nanoparticles with an average size of 30–50 nm. The biological activity of these CM-SPIONs revealed a dual and potent functionality. Multiple assays showed the nanoparticles have significantly enhanced, dose-dependent antioxidant activity, indicating a nano-bio synergy that amplifies the phytoconstituents’ effects. More importantly, this antioxidant potential translated into selective and potent anticancer efficacy against human cervical cancer (SiHa) cells. MTT assay revealed potent, dose-dependent cytotoxicity with a notably low IC50 value of 22 ± 0.7 μg/ml. Fluorescence microscopy using AO/EtBr and DAPI staining confirmed that the mechanism of cell death was predominantly apoptosis, providing initial mechanistic insight. Thus, CM-SPIONs function as an active nanotherapeutic agent, demonstrating the potential of novel plant biosystems to yield sustainable nanomedicines with dual antioxidant and pro-apoptotic efficacy.

## Linked entities

- **Diseases:** cervical cancer (MONDO:0002974)

## Full-text entities

- **Genes:** SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}
- **Diseases:** Cancer (MESH:D009369), pituitary tumour (MESH:D010911), lung cancer (MESH:D008175), neurological conditions (MESH:D019636), CC (MESH:D002583), neurological disorders (MESH:D009461), damage (MESH:D020263), alopecia (MESH:D000505), nausea (MESH:D009325), infections (MESH:D007239), cardiovascular illnesses (MESH:D002318), Cytotoxicity (MESH:D064420), necrosis (MESH:D009336), breast cancer (MESH:D001943)
- **Chemicals:** EDTA (MESH:D004492), polyethylene glycol (MESH:D011092), quercetin (MESH:D011794), clonazepam (MESH:D002998), EtBr (MESH:D004996), polyol (MESH:C024617), ferrous sulfate (MESH:C020748), 2',7'-dichlorodihydrofluorescein diacetate (MESH:C110400), streptomycin (MESH:D013307), 2, 2-diphenyl-1-picrylhydrazyl (MESH:C004931), FeCl3 (MESH:C024555), Triton X-100 (MESH:D017830), methanol (MESH:D000432), AO (MESH:D000165), metal (MESH:D008670), acridine (MESH:D000166), ferricyanide (MESH:C007931), O (MESH:D010100), Gallic acid (MESH:D005707), formazan (MESH:D005562), chitosan (MESH:D048271), magnetite (MESH:D052203), phosphate (MESH:D010710), acetic acid (MESH:D019342), Ascorbic acid (MESH:D001205), alkaloids (MESH:D000470), HCl (MESH:D006851), ferrous chloride tetrahydrate (MESH:C029451), iron oxide (MESH:C000499), hydroxyl (MESH:D017665), ethanol (MESH:D000431), free radicals (MESH:D005609), water (MESH:D014867), terpenoids (MESH:D013729), BHT (MESH:D002084), DCFH-DA (MESH:C029569), PMS (MESH:D008773), Fe (MESH:D007501), MTT (MESH:C070243), amino acids (MESH:D000596), NBT (MESH:D009580), potassium persulfate (MESH:C009007), TCA (MESH:D014238), dextran (MESH:D003911), 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MESH:C022616), Superoxide (MESH:D013481), BSS (-), H2O2 (MESH:D006861), sodium bicarbonate (MESH:D017693), K3Fe(CN)6 (MESH:C028033), penicillin (MESH:D010406), HEPES (MESH:D006531), doxorubicin (MESH:D004317), alcohols (MESH:D000438), cellulose (MESH:D002482), hydrogen (MESH:D006859), acetate (MESH:D000085), NADH (MESH:D009243), ROS (MESH:D017382), glucose (MESH:D005947)
- **Species:** Citrus sinensis (apfelsine, species) [taxon 2711], Vasconcellea monoica (col de monte, species) [taxon 262687], Carica papaya (mamon, species) [taxon 3649], Homo sapiens (human, species) [taxon 9606], Aloe vera (acibar, species) [taxon 34199], Moringa oleifera (horseradish tree, species) [taxon 3735], Hydrocotyle umbellata (species) [taxon 1475409]
- **Cell lines:** SiHa — Homo sapiens (Human), Human papillomavirus-related cervical squamous cell carcinoma, Cancer cell line (CVCL_0032), MCF-7 — Homo sapiens (Human), Invasive breast carcinoma of no special type, Cancer cell line (CVCL_0031), HEK — Homo sapiens (Human), Transformed cell line (CVCL_0045), Cos-7 monkey — Chlorocebus aethiops (Green monkey), Transformed cell line (CVCL_0224), GH3 — Rattus norvegicus (Rat), Rat pituitary gland neoplasm, Cancer cell line (CVCL_0273)

## Full text

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## Figures

15 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12917567/full.md

## References

64 references — full list in the complete paper: https://tomesphere.com/paper/PMC12917567/full.md

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Source: https://tomesphere.com/paper/PMC12917567