Evidence map›Paper›PMID 35608934›Full record

ArticleACS biomaterials science & engineering2022

Gelatin Stabilizes Nebulized Proteins in Pulmonary Drug Delivery against COVID-19.

Chunlin Li, Ira Marton, Daniel Harari, Maya Shemesh, Vyacheslav Kalchenko, Michal Pardo, Gideon Schreiber, Yinon Rudich

Open access · hybridAbstract read
In one paragraph

Article in ACS biomaterials science & engineering, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.6field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Storage stability of lysostaphin solution and its pulmonary delivery.Drug delivery and translational research · 2024
    Article
  3. Article
  4. Review
  5. Review
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Chunlin LiDepartment of Earth and Planetary Sciences, Weizmann Institute of Science, Rehovot 76100, Israel.ORCID 0000-0001-9756-5638
Ira MartonDepartment of Earth and Planetary Sciences, Weizmann Institute of Science, Rehovot 76100, Israel.
Daniel HarariDepartment of Biomolecular Sciences, Weizmann Institute of Science, Rehovot 76100, Israel.
Maya ShemeshDepartment of Biomolecular Sciences, Weizmann Institute of Science, Rehovot 76100, Israel.
Vyacheslav KalchenkoDepartment of Veterinary Resources, Weizmann Institute of Science, Rehovot 76100, Israel.
Michal PardoDepartment of Earth and Planetary Sciences, Weizmann Institute of Science, Rehovot 76100, Israel.ORCID 0000-0001-6480-1171
Gideon SchreiberDepartment of Biomolecular Sciences, Weizmann Institute of Science, Rehovot 76100, Israel.ORCID 0000-0002-2922-5882
Yinon RudichDepartment of Earth and Planetary Sciences, Weizmann Institute of Science, Rehovot 76100, Israel.ORCID 0000-0003-3149-0201
Weizmann Institute of Science · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Delivering medication to the lungs via nebulization of pharmaceuticals is a noninvasive and efficient therapy route, particularly for respiratory diseases. The recent worldwide severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) pandemic urges the development of such therapies as an effective alternative to vaccines. The main difficulties in using inhalation therapy are the development of effective medicine and methods to stabilize the biological molecules and transfer them to the lungs efficiently following nebulization. We have developed a high-affinity angiotensin-converting enzyme 2 (ACE2) receptor-binding domain (RBD-62) that can be used as a medication to inhibit infection with SARS-CoV-2 and its variants. In this study, we established a nebulization protocol for drug delivery by inhalation using two commercial vibrating mesh (VM) nebulizers (Aerogen Solo and PARI eFlow) that generate similar mist size distribution in a size range that allows efficient deposition in the small respiratory airway. In a series of experiments, we show the high activity of RBD-62, interferon-α2 (IFN-α2), and other proteins following nebulization. The addition of gelatin significantly stabilizes the proteins and enhances the fractions of active proteins after nebulization, minimizing the medication dosage. Furthermore, hamster inhalation experiments verified the feasibility of the protocol in pulmonary drug delivery. In short, the gelatin-modified RBD-62 formulation in coordination with VM nebulizer can be used as a therapy to cure SARS-CoV-2.

Indexed as

COVID-19 Drug TreatmentGelatinAerosolsHumansLungSARS-CoV-2AerosolsGelatinCoV-19gelatin stabilizationpulmonary deliveryRBD-62

Identifiers

PMID35608934
PMCPMC9159517
OpenAlexW4281381959

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.