Evidence map›Paper›PMID 42253757›Full record

ReviewInternational journal of pharmaceutics: X2026

Stabilization strategies and advancements in lyophilization to preserve integrity and efficacy of next-generation biologicals.

Ravi Maharjan, Chang Yell Shin, Seon-Kwang Lee, Eun-Sol Ha, Heejun Park, Jeong-Soo Kim, Ki Hyun Kim, Nam Ah Kim, Min-Soo Kim, Seong Hoon Jeong

Abstract readReview
In one paragraph

Review in International journal of pharmaceutics: X, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Ravi MaharjanCollege of Pharmacy and Yonsei Institute of Pharmaceutical Sciences, Yonsei University, Incheon 21983, Republic of Korea.
Chang Yell ShinDong-A ST Co. Ltd., Gyeonggi 17073, Republic of Korea.
Seon-Kwang LeeCollege of Pharmacy, Pusan National University, Busan 46241, Republic of Korea.
Eun-Sol HaCollege of Pharmacy, Pusan National University, Busan 46241, Republic of Korea.
Heejun ParkCollege of Pharmacy, Duksung Women's University, Seoul 01369, Republic of Korea.
Jeong-Soo KimCollege of Pharmacy, Duksung Women's University, Seoul 01369, Republic of Korea.
Ki Hyun KimCollege of Pharmacy, Mokpo National University, Muan 58554, Republic of Korea.
Nam Ah KimCollege of Pharmacy, Mokpo National University, Muan 58554, Republic of Korea.
Min-Soo KimCollege of Pharmacy, Pusan National University, Busan 46241, Republic of Korea.
Seong Hoon JeongCollege of Pharmacy and Yonsei Institute of Pharmaceutical Sciences, Yonsei University, Incheon 21983, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The success of mRNA-lipid nanoparticles (LNPs) vaccines during the COVID-19 pandemic has significantly increased global demand for stable, thermo-resistant biologicals. Lyophilization remains a cornerstone technology for enhancing the stability of these formulations; however, the freezing and drying processes impose major stresses that can compromise the integrity of fragile LNPs. This review systematically explores the molecular mechanisms by which lyoprotectants, including sugars, polyols, amino acids, and polymers, mitigate challenges such as ice-induced denaturation, dehydration-driven aggregation, and interfacial destabilization. This review emphasizes the importance of optimized sucrose-trehalose combinations and effective ice-nucleation control in preserving encapsulation efficiency and maintaining particle integrity. Furthermore, the review discusses advanced process optimization tools, including digital twin modeling and in-line Raman spectroscopy, which enhance lyophilization efficiency by reducing primary drying times by up to 40% while ensuring critical quality attributes are preserved. Additionally, emerging applications utilizing novel excipient combinations are highlighted, showcasing their potential to enable refrigerated storage of viral vectors. With 85% of commercial conjugates relying on lyophilization, recent advancements in continuous freeze-drying technology, such as spin-freeze approaches, have achieved cycle times that are three-fold faster. These developments provide a comprehensive roadmap for overcoming cold chain limitations while addressing the stabilization needs of next-generation biologicals, CRISPR-based systems, and personalized medicines.

Indexed as

Cold chain deliveryDigital twin modelingIce nucleationLyophilization/freeze-dryingPersonalized medicinesProcess optimizationStabilization

Identifiers

PMID42253757
PMCPMC13234487

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.