| Literature DB >> 33497928 |
Selvakumar Dharmaraj1, Veeramuthu Ashokkumar2, Sneha Hariharan3, Akila Manibharathi4, Pau Loke Show5, Cheng Tung Chong6, Chawalit Ngamcharussrivichai7.
Abstract
Recently, the COVID-19 disease spread has emerged as a worldwide pandemic and cause severe threats to humanity. The World Health Organisation (WHO) releases guidelines to help the countries to reduce the spread of this virus to the public, like wearing masks, hand hygiene, social distancing, shutting down all types of public transports, etc. These conditions led to a worldwide economic fall drastically, and on the other hand, indirect environmental benefits like global air quality improvement and decreased water pollution are also pictured. Currently, use of face masks is part of a comprehensive package of the prevention and control measures that can limit the spread of COVID-19 since there is no clinically proven drugs or vaccine available for COVID-19. Mostly, face masks are made of petroleum-based non-renewable polymers that are non-biodegradable, hazardous to the environment and create health issues. This study demonstrates the extensive use of the face mask and how it affects human health and the marine ecosystem. It has become a great challenge for the government sectors to impose strict regulations for the proper disposal of the masks as medical waste by the public. Neglecting the seriousness of this issue may lead to the release of large tonnes of micro-plastics to the landfill as well as to the marine environment where mostly end-up and thereby affecting their fauna and flora population vastly. Besides, this study highlights the COVID-19 spread, its evolutionary importance, taxonomy, genomic structure, transmission to humans, prevention, and treatment.Entities:
Keywords: COVID-19; Coronavirus; Face mask; Marine environment; Pollution
Mesh:
Year: 2021 PMID: 33497928 PMCID: PMC7836388 DOI: 10.1016/j.chemosphere.2021.129601
Source DB: PubMed Journal: Chemosphere ISSN: 0045-6535 Impact factor: 7.086
Fig. 1SARS-CoV-2 virus entry and infecting the lungs of humans causing the inflammation condition ARDS or SIRS (Alveolar cells reproduced from www.azuravesta.com).
Taxonomy of SARS-CoV-2 virus.
| Category | Virus |
|---|---|
| Orthornavirae | |
| Pisuviricota | |
| Pisoniviricetes | |
Fig. 2Structure of SARS-CoV-2 Virus (created using biorender.com).
Fig. 3SARS-CoV-2 genome organization.
Fig. 4SARS-CoV-2 virus life cycle inside the host cell.
Phase 3 clinical trials of COVID-19 Vaccines (www.raps.org).
| S. No. | Vaccine Developer | Candidate | Mechanism | Current Status |
|---|---|---|---|---|
| 1. | Moderna; Kaiser Permanente Washington Health Research Institute. | mRNA-1273 | mRNA-based vaccine | On 12 May, mRNA-1273 was granted Fast Track designation by the FDA. A Phase 3 vaccine trial is underway and is being funded by OWS. The Medicines and Healthcare Products Regulatory Agency (MHRA) of the United Kingdom has begun a real-time analysis of mRNA-1273, which will allow a faster vaccine approval process. |
| 2. | Sinovac; Sinovac Research and Development Co., Ltd. | CoronaVac | Inactivated vaccine (formalin with alum adjuvant) | Sinovac representatives told Reuters that the vaccine appeared to be effective for older participants in the trial and did not cause any significant side effects. Preliminary findings from the Instituto Butantan trial announced by the company suggest that CoronaVac has so far been safe and no significant adverse reactions have been identified. Owing to a patient death, the trial in Brazil was briefly suspended, but the trial has later resumed. |
| 3. | Bharat Biotech; National Institute of Virology | Covaxin | Inactivated vaccine | According to an ICMR scientist who spoke to Reuters, the vaccine could begin distribution as early as February 2021. |
| 4. | Pfizer; BioNTech | BNT162 | mRNA-based vaccine | For BNT162b1 and BNT162b2, Pfizer and BioNTech have secured the Fast Track designation from the FDA. Based on the totality of available evidence from our preclinical and clinical trials, including selected immune response and tolerability parameters, BNT162b2 was chosen to progress to a Phase 2/3 safety review. The companies also requested the FDA to consider an extended procedure to include up to 44,000 participants for the Phase 3 trial. European Medicines Agency (EMA) has launched a rolling review of BNT162b2, which may accelerate the candidate’s approval. According to the Wall Street Journal, Pfizer and BioNTech may be able to file for an Emergency Use Authorizations (EUA) in November and have the vaccine ready for use in December. In Australia, the Australian Therapeutic Goods Administration (TGA) provided BNT162b2 with a provisional determination, which is the first step on the path to approval of the vaccine in the region. Shanghai Fosun Pharmaceutical Company, BioNTech’s partner in China announced that it was seeking approval for BNT162b2 in China but would no longer conducting BNT162b1 clinical trials. |
| 5. | The University of Oxford; AstraZeneca; IQVIA; Serum Institute of India | AZD1222 | Replication-deficient viral vector vaccine (adenovirus from chimpanzees) | In part, the Biomedical Advanced Research and Development Authority (BARDA) and OWS are financing the AstraZeneca trials. IQVIA has announced that they are working with AstraZeneca to advance the vaccine’s clinical trials. In the United States and at study sites in India, phase 3 studies are being conducted, but have been put on hold following a serious adverse event. Trials have since resumed. The Human Medicines Committee (CHMP) of EMA has begun a rolling review of AZD1222 to decrease the amount of time before a safety and efficacy decision is taken, as has Health Canada. The Australian Therapeutic Good Administration (TGA) granted the provisional determination of AZD1222 in Australia, the first step in the approval process. An accelerated analysis of AZD1222 in Britain has also been initiated by the Medicines and Healthcare products Regulatory Agency (MHRA). |
| 6. | Johnson and Johnson | NJ-78436735 | Non-replicating viral vector | Johnson and Johnson announced on 10th June 2020, that it is accelerating Phase 1/2 trials and that human trials are underway. According to the firm, the Phase 3 study, estimated to enrol up to 60,000 individuals, is also under way. The ENSEMBLE research was on hold pending a review of an adverse condition developed by a participant in one of the study arms, but after the Independent Data Protection and Monitoring Board recommended the trial restart recruiting, Johnson and Johnson was cleared to resume the trial in the U.S. and Brazil. Johnson and Johnson said it expects as soon as possible to begin testing its vaccine in adolescents. |
| 7. | Wuhan Institute of Biological Products; China National Pharmaceutical Group (Sinopharm) | Not named | Inactivated vaccine | In Peru, Morocco, and the United Arab Emirates, a Phase 3 trial is underway. |
| 8. | Novavax | NVX-CoV2373 | Nanoparticle vaccine | Novavax has received the NVX-CoV2373Fast Track Designation from the FDA. The Coalition for Epidemic Preparedness Innovations (CEPI) announced on 11th May 2020, that it had provided Novavax with an additional $384 million to develop and produce NVX-CoV2373. As part of its recent acquisition of Praha Vaccines, Novavax plans to produce 1 billion doses of NVX-CoV2373 by 2021. According to a company press release, Novavax was awarded a $60 million by US Department of Defense contract to produce NVX-CoV2373, and another $1.6 billion from Operation Warp Speed if the candidate is successful in clinical trials. The candidate has formally initiated a Phase 3 trial in the United Kingdom to test the vaccine for up to 10,000 participants, the company said in a press release. Novavax updated its Phase 3 trial of NVX-CoV2373 in North America on 27th October 2020, announcing that the trial will begin at the end of November, approximately one month later than anticipated. |
| 9. | Gamaleya Research Institute; Acellena Contract Drug Research and Development. | Sputnik V | Non-replicating viral vector | The Russian Federation’s Health Ministry has approved Sputnik V as the first COVID-19 vaccine. To date, however no trial information has been released. Due to a lack of safety and efficacy evidence, the approval has drawn controversy in the medical community. In Brazil, the Institute has made a preliminary pre-submission of the vaccine appropriate for its use in the region. |
| 10. | CanSino Biologics; Tongji Hospital; Wuhan, China. | Ad5-nCoV | Recombinant vaccine (adenovirus type 5 vector) | As reported to Reuters on 25 June by the Central Military Commission of China announced that the military had been allowed to use Ad5-nCoV for a duration of one year. |
Fig. 5Different types of Masks that are currently in use as well as in research stage (Das et al., 2020, reproduced with permission).
Different types of Masks and its uses.
| TYPES OF MASKS | SURGICAL MASK | CLOTH MASKS | N95 RESPIRATORS | REFERENCES |
|---|---|---|---|---|
| European Standard EN 14683:2019 + AC: 2019, ASTM | None | European Standard EN 149:2001 + A1: 2009, NIOSH-42CFR84 in the United States, GB2626-2006 in China. | ||
| Fluid resistant and protects wearer from large droplets, splashes and bodily fluids | Helps protect others from you, not fluid resistant | Reduces wearer’s exposure to airborne particles including small particle aerosols and large fluid droplets. | ||
| Breathable | Breathable | Difficult | ||
| Non-Woven Fabric Polypropylene 3 Layers - Outer Layer-Hydrophobic Non-Woven layer, Middle layer - Melt blown filter, Inner layer -Soft absorbent Non-Woven layer | Cotton | 1st layer - Spun-bond polypropylene | ||
| Leakage through mask edges | Leakage occurs throughout cloth | Minimal leakage. When [properly fitted and worn] | ||
| Loose-fitted | Loose-fitted | Tight-fitted | ||
| Moderate level filtration | Low level filtration | High level filtration | ||
| Disposable/Single use | Re-useable | Discard after each use, |
Fig. 6Present and future plastic pollutants that exist in coastal and marine environment.