# A Membrane‐Targeting Photosensitizer with Aggregation‐Induced Emission Characteristics for Highly Efficient Photodynamic Combat of Human Coronaviruses

**Authors:** Ming‐Yu Wu, Meijia Gu, Jong‐Kai Leung, Xinmei Li, Yuncong Yuan, Chao Shen, Lianrong Wang, Engui Zhao, Sijie Chen

PMC · DOI: 10.1002/smll.202101770 · Small (Weinheim an Der Bergstrasse, Germany) · 2021-06-30

## TL;DR

A new photosensitizer called DTTPB can efficiently inactivate human coronaviruses using light, offering a promising method to combat the spread of COVID-19.

## Contribution

The novel photosensitizer DTTPB with aggregation-induced emission characteristics is introduced for photodynamic inactivation of human coronaviruses.

## Key findings

- DTTPB effectively targets and binds to the envelope of human coronaviruses.
- Upon light irradiation, DTTPB inactivates human coronaviruses, leading to a complete loss of infectivity.
- DTTPB demonstrates high molar absorptivity and broad visible light absorption, making it suitable for photodynamic therapy.

## Abstract

COVID‐19 pandemic, caused by severe acute respiratory syndrome coronavirus 2, has resulted in global social and economic disruption, putting the world economy to the largest global recession since the Great Depression. To control the spread of COVID‐19, cutting off the transmission route is a critical step. In this work, the efficient inactivation of human coronavirus with photodynamic therapy (PDT) by employing photosensitizers with aggregation‐induced emission characteristics (DTTPB) is reported. DTTPB is designed to bear a hydrophilic head and two hydrophobic tails, mimicking the structure of phospholipids on biological membranes. DTTPB demonstrates a broad absorption band covering the whole visible light range and high molar absorptivity, as well as excellent reactive oxygen species sensitizing ability, making it an excellent candidate for PDT. Besides, DTTPB can target membrane structure, and bind to the envelope of human coronaviruses. Upon light irradiation, DTTPB demonstrates highly effective antiviral behavior: human coronavirus treated with DTTPB and white‐light irradiation can be efficiently inactivated with complete loss of infectivity, as revealed by the significant decrease of virus RNA and proteins in host cells. Thus, DTTPB sensitized PDT can efficiently prevent the infection and the spread of human coronavirus, which provides a new avenue for photodynamic combating of COVID‐19.

In this work, we report the application of a novel photosensitizer, DTTPB, with aggregation‐induced emission characteristics for photodynamic inactivation of human coronaviruses. With high molar absorbance coefficient, broad absorption band covering the whole white light region, and high membrane targeting and ROS sensitizing efficiency, DTTPB could effectively inactivate human coronaviruses and may contribute to preventing the spread of COVID‐19 pandemic.

## Linked entities

- **Diseases:** COVID-19 (MONDO:0100096), severe acute respiratory syndrome coronavirus 2 (MONDO:0100096)

## Full-text entities

- **Diseases:** infectious pathogens (MESH:D003141), infected (MESH:D007239), Cytotoxicity (MESH:D064420), liver carcinoma (MESH:D006528), death (MESH:D003643), cervical carcinoma (MESH:D002583), Depression (MESH:D003866), coronavirus (MESH:D018352), CPE (MESH:D065606), COVID-19 (MESH:D000086382), tumor (MESH:D009369), Viral Titering (MESH:D014777)
- **Chemicals:** porphyrins (MESH:D011166), carbon (MESH:D002244), TRITC (MESH:C009434), diketopyrrolopyrroles (MESH:C000604894), ROS (MESH:D017382), Ethanol (MESH:D000431), lipid (MESH:D008055), aldehyde (MESH:D000447), 1,2-dioleoyl-sn-glycero-3-phosphocholine (MESH:C017251), phthalocyanines (MESH:C013647), DMSO (MESH:D004121), hypochlorite (MESH:D006997), phospholipid (MESH:D010743), PBS (MESH:D007854), 2',7'-dichlorodihydrofluorescein diacetate (MESH:C110400), T (MESH:D014316), 1O2 (-), RB (MESH:D012395), toluene (MESH:D014050),  (MESH:D017319)
- **Species:** Orthocoronavirinae (subfamily) [taxon 2501931], Gammacoronavirus (genus) [taxon 694013], Human coronavirus OC43 (no rank) [taxon 31631], Human coronavirus 229E (no rank) [taxon 11137], Mus musculus (house mouse, species) [taxon 10090], Foot-and-mouth disease virus (no rank) [taxon 12110], Cricetus cricetus (black-bellied hamster, species) [taxon 10034], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** HeLa — Homo sapiens (Human), Human papillomavirus-related cervical squamous cell carcinoma, Cancer cell line (CVCL_T292), HEK-293T — Homo sapiens (Human), Transformed cell line (CVCL_0063), MRC-5 — Homo sapiens (Human), Finite cell line (CVCL_0440), BHK-21 — Mesocricetus auratus (Golden hamster), Spontaneously immortalized cell line (CVCL_RQ70), HepG2 — Homo sapiens (Human), Hepatoblastoma, Cancer cell line (CVCL_0027), NIH-3T3 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0594)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC8420407/full.md

## References

44 references — full list in the complete paper: https://tomesphere.com/paper/PMC8420407/full.md

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Source: https://tomesphere.com/paper/PMC8420407