# Integrated GC–MS Profiling and Phytosynthesis of MnO2 Nanoparticles Using Moringa oleifera: Assessment of Antioxidant, Cytotoxicity, and Potential In Vitro and In Silico Inhibitory Effects on α‐Amylase and α‐Glucosidase

**Authors:** Selokela Joseph Mahlo, Adewale Odunayo Oladipo, Mpho Phehello Ngoepe, Yvan Anderson Ngandjui Tchangoue, Titus Alfred Makudali Msagati, Sogolo Lucky Lebelo, Garland Kgosi More

PMC · DOI: 10.1002/cbdv.202503171 · Chemistry & Biodiversity · 2026-02-25

## TL;DR

Researchers used Moringa oleifera to create MnO2 nanoparticles with strong antioxidant and antidiabetic properties, showing low toxicity and potential therapeutic applications.

## Contribution

The study introduces a novel phytosynthesis method for MnO2 nanoparticles using Moringa oleifera and evaluates their antioxidant, cytotoxic, and antidiabetic properties.

## Key findings

- MnO2 nanoparticles synthesized from Moringa oleifera are spherical, crystalline, and about 8.3 nm in size.
- The nanoparticles showed strong antioxidant activity with IC50 values of 9.08 and 6.62 µg/mL in DPPH and ABTS assays.
- They exhibited significant antidiabetic effects against α-amylase and α-glucosidase enzymes with IC50 values of 36.58 and 55.03 µg/mL, respectively.

## Abstract

Bioactive compounds from medicinal plants can enhance the therapeutic potential of trace metal–oxide nanoparticles. This study contributed to identifying the main volatile compounds and synthesizing manganese dioxide nanoparticles (MnO2 NPs) using Moringa oleifera (MO) leaf extract and explored their biological applications. Gas chromatography–mass spectrometry (GC–MS) analysis identified 21 volatile compounds with known bioactivities from the leaves of MO. Transmission electron microscopy (TEM) and x‐ray diffraction analysis showed that MnO2 NPs were spherical and crystalline, averaging ∼8.3 nm in size. Antioxidant activity, assessed by 2,2‐diphenyl‐1‐picrylhydrazyl (DPPH) and 2,2′‐azino‐bis (3‐ethylbenzothiazoline‐6‐sulfonic acid) (ABTS) assays, revealed high potency (IC50 = 9.08 ± 0.11 and 6.62 ± 0.12 µg/mL). Cell viability assays indicated relative non‐toxicity, with IC50 values greater than 20 µg/mL for human embryonic kidney (HEK 293) and liver (HEPG2) cells. The antidiabetic effects were evaluated against α‐amylase and α‐glucosidase enzymes, showing IC50 values of 36.58 ± 0.74 and 55.03 ± 1.68 µg/mL, respectively, compared to FDA‐approved acarbose. Docking studies yielded scores of −6.10 and −7.32 kcal/mol. Overall, these results highlight that the MO‐synthesized MnO2 NPs can be explored as potential antioxidant, cytoprotective, and antidiabetic agents for therapeutic uses.

Manganese oxide (MnO NPs), synthesis of Moringa oleifera leaf extract nanoparticles, are spherical and crystalline with a size of 8.3 nm. They exhibit strong antioxidant activity in DPPH and ABTS assays, with IC50 values of 9.08 and 6.62 µg/mL, respectively, and demonstrate low toxicity to kidney and liver cells. MnO NPs also show significant antidiabetic effects against α‐amylase and α‐glucosidase, suggesting their potential as antioxidants, cytoprotective, and antidiabetic agents.

## Linked entities

- **Chemicals:** ABTS (PubChem CID 35688), acarbose (PubChem CID 9811704), MnO2 (PubChem CID 14801)
- **Species:** Moringa oleifera (taxon 3735)

## Full-text entities

- **Genes:** AMY2A (amylase alpha 2A) [NCBI Gene 279] {aka AMY2, PA}, AMYA1 (alpha-amylase) [NCBI Gene 102577485] {aka amyA2}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, SI (sucrase-isomaltase) [NCBI Gene 6476]
- **Diseases:** glucose intolerance (MESH:D018149), hepatocellular carcinoma (MESH:D006528), Type 1 diabetes (MESH:D003922), hepatic toxicity (MESH:D056486), breast cancer (MESH:D001943), Type 2 diabetes (MESH:D003924), manganese (MESH:D020149), Cytotoxicity (MESH:D064420), gastrointestinal complications (MESH:D005767), viral and bacterial infections (MESH:D014777), hypertension (MESH:D006973), male and female infertility (MESH:D007248), diarrhea (MESH:D003967), acute pancreatitis (MESH:D010195), abdominal pain (MESH:D015746), DM (MESH:D003920), cancer (MESH:D009369), ND (MESH:C537849), renal and liver failure (MESH:D051437), neurotoxicity (MESH:D020258), pain (MESH:D010146), Hyperglycemia (MESH:D006943), inflammation (MESH:D007249)
- **Chemicals:** saponins (MESH:D012503), glycosides (MESH:D006027), Manganese (MESH:D008345), glucose (MESH:D005947), voglibose (MESH:C102817), magnesium (MESH:D008274), DMSO (MESH:D004121), flavonoids (MESH:D005419), alcohol (MESH:D000438), hydrogen (MESH:D006859), PBS (MESH:D007854), alpha-tocopherol (MESH:D024502), Na2CO3 (MESH:C005686), hexadecanoic acid (MESH:D019308), 2,2'-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid (MESH:C002502), magnesium oxide (MESH:D008277), CO2 (MESH:D002245), K2S2O8 (MESH:C009007), carbohydrates (MESH:D002241), saturated fatty acids (MESH:D005227), oils (MESH:D009821), selenium (MESH:D012643), p-nitrophenol (MESH:C024836), MTT (MESH:C070243), amino acids (MESH:D000596), tetracosane (MESH:C514857), Cholesta-3,5-diene (MESH:C076149), penicillin (MESH:D010406), Doxorubicin (MESH:D004317), curcumin (MESH:D003474), helium (MESH:D006371), nickel oxide (MESH:C028007), 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MESH:C022616), Acarbose (MESH:D020909), 1,3,5-triphenyl- (-), DNS (MESH:C022306), blood sugar (MESH:D001786), cholesterol (MESH:D002784), cyclohexane (MESH:C506365), meglitinides (MESH:C030516), Ascorbic acid (MESH:D001205), alkaloids (MESH:D000470), Cu (MESH:D003300), Manganese oxide (MESH:C027424), alkanes (MESH:D000473), biguanides (MESH:D001645), Sulphonylurea (MESH:D013453), terpenoids (MESH:D013729), alkenes (MESH:D000475), iron (MESH:D007501), cobalt oxide (MESH:C060728), metformin (MESH:D008687), cerium oxide (MESH:C030583), MnO2 (MESH:C016552), amides (MESH:D000577), water (MESH:D014867), streptomycin (MESH:D013307), C (MESH:D002244), thiazolidinedione (MESH:C089946), 2,2-diphenyl-1-picrylhydrazyl (MESH:C004931)
- **Species:** Homo sapiens (human, species) [taxon 9606], Moringa oleifera (horseradish tree, species) [taxon 3735], Microbacterium sp. O (species) [taxon 2502250], Lagerstroemia speciosa (giant crepe-myrtle, species) [taxon 122810], Hibiscus rosa-sinensis (Chinese hibiscus, species) [taxon 183298]
- **Cell lines:** N27 — Rattus norvegicus (Rat), Transformed cell line (CVCL_D584), HEK 293 — Homo sapiens (Human), Transformed cell line (CVCL_0045), PC-12 — Rattus norvegicus (Rat), Rat adrenal gland pheochromocytoma, Cancer cell line (CVCL_0481), MDA-MB-231 — Homo sapiens (Human), Breast adenocarcinoma, Cancer cell line (CVCL_0062), MCF-7 — Homo sapiens (Human), Invasive breast carcinoma of no special type, Cancer cell line (CVCL_0031), ATCC HB8065 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023), CRL-1573 — Sigmodon hispidus (Hispid cotton rat), Spontaneously immortalized cell line (CVCL_YD58), HEPG2 — Homo sapiens (Human), Hepatoblastoma, Cancer cell line (CVCL_0027)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12935285/full.md

## References

75 references — full list in the complete paper: https://tomesphere.com/paper/PMC12935285/full.md

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Source: https://tomesphere.com/paper/PMC12935285