Evidence map›Paper›PMID 40109738›Full record

ArticleACS pharmacology & translational science2025

Safe-by-Design Strategies for Intranasal Drug Delivery Systems: Machine and Deep Learning Solutions to Differentiate Epithelial Tissues via Attenuated Total Reflection Fourier Transform Infrared Spectroscopy.

Romain Topalian, Leo Kavallaris, Frank Rosenau, Chrystelle Mavoungou

Abstract read
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Article in ACS pharmacology & translational science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

4 authors.

Romain TopalianInstitute for Applied Biotechnology, Biberach University of Applied Sciences, Karlstraße 6-11, 88400 Biberach, Germany.ORCID https://orcid.org/0009-0002-0436-3856
Leo KavallarisInstitute for Applied Biotechnology, Biberach University of Applied Sciences, Karlstraße 6-11, 88400 Biberach, Germany.
Frank RosenauInstitute of Pharmaceutical Biotechnology, Ulm University, Albert-Einstein-Allee 11, 89081 Ulm, Germany.ORCID https://orcid.org/0000-0002-9297-6419
Chrystelle MavoungouInstitute for Applied Biotechnology, Biberach University of Applied Sciences, Karlstraße 6-11, 88400 Biberach, Germany.ORCID https://orcid.org/0000-0002-8122-1248

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of nasal drug delivery systems requires advanced analytical techniques and tools that allow for distinguishing between the nose-to-brain epithelial tissues with better precision, where traditional bioanalytical methods frequently fail. In this study, attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy is coupled to machine learning (ML) and deep learning (DL) techniques to discriminate effectively between epithelial tissues. The primary goal of this work was to develop Safe-by-Design models for intranasal drug delivery using ex vivo pig tissues experiment, which were analyzed by way of ML modeling. We compiled an ATR-FTIR spectral data set from olfactory epithelium (OE), respiratory epithelium (RE), and tracheal tissues. The data set was used to train and test different ML algorithms. Accuracy, sensitivity, specificity, and F1 score metrics were used to evaluate optimized model performance and their abilities to identify specific spectral signatures relevant to each tissue type. The used feedforward neural network (FNN) has shown 0.99 accuracy, indicating that it had performed a discrimination with a high level of trueness estimates, without overfitting, unlike the built support vector machine (SVM) model. Important spectral features detailing the assignment and site of two-dimensional (2D) protein structures per tissue type were determined by the SHapley Additive exPlanations (SHAP) value analysis of the FNN model. Furthermore, a denoising autoencoder was built to improve spectral quality by reducing noise, as confirmed by higher Pearson correlation coefficients for denoised spectra. The combination of spectroscopic analysis with ML modeling offers a promising strategy called, Safe-by-Design, as a monitoring strategy for intranasal drug delivery systems, also for designing the analysis of tissue for diagnosis purposes.

Identifiers

PMID40109738
PMCPMC11915033

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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.