# Carbon nanodots as theranostics agents in cancer: advances in design, targeting, and real-time monitoring

**Authors:** Mayank Kumar, Manini Bhatt, Bodhisatwa Das

PMC · DOI: 10.1039/d5ra07928d · RSC Advances · 2026-02-18

## TL;DR

Carbon nanodots are being developed as a powerful tool for both diagnosing and treating cancer with reduced toxicity and improved imaging capabilities.

## Contribution

This review highlights recent advances in the design and application of carbon nanodots for cancer theranostics, emphasizing their multimodal capabilities and future directions.

## Key findings

- Carbon nanodots offer deep-tissue imaging and targeted therapy with reduced toxicity.
- Recent developments include multimodal imaging and light-activated therapies using CNDs.
- Challenges remain in biosafety, scalability, and regulatory readiness for clinical use.

## Abstract

Carbon nanodots (CNDs) have emerged as a promising class of carbon-based nanomaterials for cancer theranostics, uniquely integrating diagnosis and therapy on a single platform. Their ultrasmall size, high aqueous dispersibility, tunable photoluminescence extending into the near-infrared (NIR) window, and compatibility with green, scalable synthesis enable deep-tissue imaging and targeted intervention with reduced systemic toxicity compared with many conventional nanomaterials. This review summarises recent advances in the top-down and bottom-up fabrication of CNDs, including heteroatom doping and surface functionalisation with ligands or stimuli-responsive linkers, and relates these design parameters to optical performance, tumour selectivity, and responsiveness to the tumour microenvironment. Particular emphasis is placed on CND-based platforms for multimodal imaging (fluorescence, MRI, and photoacoustic), controlled-release drug delivery, gene silencing, and light-activated photodynamic and photothermal therapies, as well as emerging synergistic systems that combine these functions for real-time, image-guided treatment. Remaining challenges, such as batch-to-batch variability, incomplete understanding of long-term biosafety (especially for metal-doped CNDs), and limited clinical-scale manufacturing and regulatory readiness, are critically discussed alongside future opportunities, including NIR-II optimisation, protein-corona-resistant surface engineering, and AI-assisted CND design for personalised cancer theranostics.

This review focuses on carbon nanodots as a theragnostic probe for multimodal imaging and disease diagnosis, and therapeutic nanoprobe with various application windows.

## Linked entities

- **Diseases:** cancer (MONDO:0004992)

## Full-text entities

- **Genes:** CND (Corneal dermoids) [NCBI Gene 8231], EREG (epiregulin) [NCBI Gene 2069] {aka EPR, ER, Ep}, CD44 (CD44 molecule (IN blood group)) [NCBI Gene 960] {aka CDW44, CSPG8, ECM-III, ECMR-III, H-CAM, HCELL}, BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581] {aka BCL2L4}, CEACAM3 (CEA cell adhesion molecule 3) [NCBI Gene 1084] {aka CD66D, CEA, CGM1, CGM1a, W264, W282}, CTSB (cathepsin B) [NCBI Gene 1508] {aka APPS, CPSB, KWE, RECEUP}, AFP (alpha fetoprotein) [NCBI Gene 174] {aka AFPD, FETA, HPAFP}, APAF1 (apoptotic peptidase activating factor 1) [NCBI Gene 317] {aka APAF-1, CED4}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}, ALK (ALK receptor tyrosine kinase) [NCBI Gene 238] {aka ALK1, CD246, NBLST3}, ITGAV (integrin subunit alpha V) [NCBI Gene 3685] {aka CD51, IDNDC, MSK8, VNRA, VTNR}, BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}, TF (transferrin) [NCBI Gene 7018] {aka HEL-S-71p, PRO1557, PRO2086, TFQTL1}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, FAS (Fas cell surface death receptor) [NCBI Gene 355] {aka ALPS1A, APO-1, APT1, CD95, FAS1, FASTM}, AR (androgen receptor) [NCBI Gene 367] {aka AIS, AR8, DHTR, HPCX3, HUMARA, HYSP1}, BID (BH3 interacting domain death agonist) [NCBI Gene 637] {aka FP497}, RTN4R (reticulon 4 receptor) [NCBI Gene 65078] {aka NGR, NOGOR, NgR1}, KRAS (KRAS proto-oncogene, GTPase) [NCBI Gene 3845] {aka 'C-K-RAS, C-K-RAS, CFC2, K-RAS2A, K-RAS2B, K-RAS4A}, CTSD (cathepsin D) [NCBI Gene 1509] {aka CLN10, CPSD, HEL-S-130P}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, FADD (Fas associated via death domain) [NCBI Gene 8772] {aka GIG3, IMD90, MORT1}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, CASP3 (caspase 3) [NCBI Gene 836] {aka CPP32, CPP32B, SCA-1}, CASP9 (caspase 9) [NCBI Gene 842] {aka APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56}, MIR21 (microRNA 21) [NCBI Gene 406991] {aka MIRN21, hsa-mir-21, miR-21, miRNA21}, FOLH1 (folate hydrolase 1) [NCBI Gene 2346] {aka FGCP, FOLH, GCP2, GCPII, NAALAD1, PSM}, NUCLEOLIN (nucleolin multifunctional protein) [NCBI Gene 4691] {aka C23, NCL, Nsr1}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, KLK3 (kallikrein related peptidase 3) [NCBI Gene 354] {aka APS, KLK2A1, PSA, hK3}, CYCS (cytochrome c, somatic) [NCBI Gene 54205] {aka CYC, HCS, THC4}, BCL2L11 (BCL2 like 11) [NCBI Gene 10018] {aka BAM, BIM, BOD}, BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673] {aka B-RAF1, B-raf, BRAF-1, BRAF1, NS7, RAFB1}, EPCAM (epithelial cell adhesion molecule) [NCBI Gene 4072] {aka Ber-Ep4, BerEp4, DIAR5, EGP-2, EGP314, EGP40}, ANPEP (alanyl aminopeptidase, membrane) [NCBI Gene 290] {aka AP-M, AP-N, APN, CD13, GP150, LAP1}, HIF1A (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 3091] {aka HIF-1-alpha, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, CYP19A1 (cytochrome P450 family 19 subfamily A member 1) [NCBI Gene 1588] {aka ARO, ARO1, CPV1, CYAR, CYP19, CYPXIX}
- **Diseases:** inflammatory changes (MESH:D007249), metastases (MESH:D009362), prostate cancer (MESH:D011471), fibrosis (MESH:D005355), mouth ulcers (MESH:D019226), deaths (MESH:D003643), cystic lesions (MESH:D052177), demyelinating lesions in the central nervous system (MESH:D003711), mitochondrial dysfunction (MESH:D028361), pancreatic cancer (MESH:D010190), colorectal cancer (MESH:D015179), nerve damage (MESH:D000080902), infection (MESH:D007239), lung cancer (MESH:D008175), endocrinopathies (MESH:C567425), CD (MESH:D003424), oedema (MESH:C536897), CDT (MESH:C537067), colitis (MESH:D003092), Cancer (MESH:D009369), gastrointestinal (MESH:D005767), cytotoxicity (MESH:D064420), CNDs (MESH:D002249), axonal degeneration (MESH:D009410), bleeding (MESH:D006470), mucositis (MESH:D052016), Breast cancer (MESH:D001943), hypoxic (MESH:D002534), organ failure (MESH:D009102), peripheral nerve pain (MESH:D009437), alopecia (MESH:D000505), androgen limitation (MESH:D014770), Fatigue (MESH:D005221), Pneumonia (MESH:D011014), diarrhoea (MESH:D003967), soreness (MESH:D063806), I (MESH:D006969), cardiotoxicity (MESH:D066126), necrosis (MESH:D009336), melanoma, lung, and hematologic tumours (MESH:D019337), hyperthermia (MESH:D005334), II ROS (MESH:D000860), prostate (MESH:D011472)
- **Chemicals:** CNDs (-), superoxide (MESH:D013481), metal (MESH:D008670), porphyrins (MESH:D011166), Platinum (MESH:D010984), cisplatin (MESH:D002945), graphite (MESH:D006108), exemestane (MESH:C056516), gold (MESH:D006046), Gd3 (MESH:C026226), S (MESH:D013455), curcumin (MESH:D003474), singlet oxygen (MESH:D026082), chlorins (MESH:C006969), P (MESH:D010758), salt (MESH:D012492), DOX (MESH:D004317), nitriles (MESH:D009570), acid- (MESH:D000143), anthracyclines (MESH:D018943), RGD (MESH:C047981), imine (MESH:D007097), disulfide (MESH:D004220), letrozole (MESH:D000077289), oxygen (MESH:D010100), Tamoxifen (MESH:D013629), thiol (MESH:D013438), graphene oxide (MESH:C000628730), oestradiol (MESH:D004958), CO (MESH:D002248), lactic acid (MESH:D019344), N (MESH:D009584), CNTs (MESH:D037742), vincristine (MESH:D014750), paclitaxel (MESH:D017239), amine (MESH:D000588), hydroxyapatite (MESH:D017886), polymer (MESH:D011108), arginine (MESH:D001120), acetone (MESH:D000096), C (MESH:D002244), FeO4 (MESH:C020748), Vinca alkaloids (MESH:D014748), water (MESH:D014867), Gd (MESH:D005682), 5-fluorouracil (MESH:D005472), amide (MESH:D000577), enzalutamide (MESH:C540278), hydrazone (MESH:D006835), GSH (MESH:D005978), AS1411 (MESH:C513936), Taxanes (MESH:D043823), testosterone (MESH:D013739), anastrozole (MESH:D000077384), carbodiimide (MESH:D002234), FL (MESH:D005459), OH (MESH:C031356), gemcitabine (MESH:D000093542), Cu (MESH:D003300), Mn (MESH:D008345)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** 4T1 — Mus musculus (Mouse), Malignant neoplasms of the mouse mammary gland, Cancer cell line (CVCL_0125), A549 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023), CT26 — Mus musculus (Mouse), Mouse colon adenocarcinoma, Cancer cell line (CVCL_7254), HeLa — Homo sapiens (Human), Human papillomavirus-related endocervical adenocarcinoma, Cancer cell line (CVCL_0030), DU145 — Homo sapiens (Human), Prostate carcinoma, Cancer cell line (CVCL_0105)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12915097/full.md

## References

107 references — full list in the complete paper: https://tomesphere.com/paper/PMC12915097/full.md

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Source: https://tomesphere.com/paper/PMC12915097