# Enhancing optical properties and stability of DNA-functionalized carbon nanotubes with cryoprotectant-mediated lyophilization

**Authors:** Aceer Nadeem, Aidan Kindopp, Ella Junge, Maryam Rahmani, Daniel Roxbury

PMC · DOI: 10.1016/j.carbon.2025.121159 · 2026-02-05

## TL;DR

This paper shows how using specific cryoprotectants during freeze-drying improves the stability and optical performance of DNA-coated carbon nanotubes for biomedical applications.

## Contribution

The study introduces an optimized lyophilization method with glucose-PEG cryoprotectants to enhance DNA-SWCNT stability and reusability.

## Key findings

- Glucose and PEG in an 80:20 ratio best preserved NIR fluorescence and prevented SWCNT aggregation.
- Lyophilized SWCNTs with glucose-PEG showed stable intracellular optical performance in murine macrophages.
- The method improves shelf life and reproducibility of DNA-SWCNT sensors for biomedical use.

## Abstract

The long-term optical performance and stability of single-walled carbon nanotubes (SWCNTs) functionalized with single-stranded DNA are critical for their application in near-infrared (NIR) fluorescence biological sensing and imaging. However, the aggregation of such DNA-SWCNTs during storage presents a significant challenge. Here, we explored the use of lyophilization combined with various cryoprotectants to enhance the long-term stability and reconstitution of DNA-SWCNTs at room temperature. Five conventionally used cryoprotectants, including glucose, sucrose, mannitol, polyethylene glycol (PEG), and polyvinyl alcohol (PVA), were evaluated for their ability to maintain desired optical properties and prevent aggregation of SWCNTs through the process of lyophilization and reconstitution. Our results indicated that glucose and PEG, particularly in an 80:20 ratio by weight, provided the best performance, preserving NIR fluorescence and ensuring consistent reconstitution without significant aggregation. Further, in vitro studies using murine macrophages demonstrated that lyophilized SWCNTs with glucose-PEG protectants and then held at room temperature before subsequent reconstitution maintained stable intracellular optical performance, supporting their potential for long-term storage, ease of transport, and use in biomedical applications. These findings suggest that the optimized lyophilization protocol with specific cryoprotectant combinations can significantly improve the shelf life and reproducibility of SWCNT-based sensors, paving the way for their broader application in biological and clinical settings.

## Linked entities

- **Chemicals:** glucose (PubChem CID 5793), sucrose (PubChem CID 5988), mannitol (PubChem CID 6251), polyethylene glycol (PubChem CID 9033), PEG (PubChem CID 174), PVA (PubChem CID 11199)

## Full-text entities

- **Chemicals:** mannitol (MESH:D008353), penicillin (MESH:D010406), carbon (MESH:D002244), streptomycin (MESH:D013307), DMSO (MESH:D004121), carbon nanotubes (MESH:D037742), polymer (MESH:D011108), graphene (MESH:D006108), glycerol (MESH:D005990), O (MESH:D010100), Sucrose (MESH:D013395), ice (MESH:D007053), CO2 (MESH:D002245), amphotericin B (MESH:D000666), HEPES (MESH:D006531), hydrogen (MESH:D006859), NaCl (MESH:D012965), hydrogen peroxide (MESH:D006861), water (MESH:D014867), lipid (MESH:D008055), gold (MESH:D006046), ethylene glycol (MESH:D019855), Glucose (MESH:D005947), Sugar (MESH:D000073893), sugar alcohol (MESH:D013402), HiPCO (-), PEG (MESH:D011092), l-glutamine (MESH:D005973), PVA (MESH:D011142)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** RAW 264.7 — Mus musculus (Mouse), Mouse leukemia, Cancer cell line (CVCL_0493), TIB-71 — Homo sapiens (Human), Cri du chat syndrome, Finite cell line (CVCL_4150), D-10 — Mus musculus (Mouse), Factor-dependent cell line (CVCL_0241), SWCNTs — Gallus gallus (Chicken), Spontaneously immortalized cell line (CVCL_C3NY)

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12872225/full.md

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Source: https://tomesphere.com/paper/PMC12872225