<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE317nnn/GSE317613/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE317613</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>pH-Responsive Nanostructured Calcium Phosphate Microrods as Pulmonary Delivery Platform: Fabrication, Characterization, and Comparative Assessment of Cytotoxic and Transcriptomic Responses in Alveolar Macrophages</name><description>Nanostructured, rod-shaped microparticles represent a promising drug-delivery plat-form for pulmonary delivery and targeting of alveolar macrophage by leveraging the aerodynamic advantages of fiber-like geometries. These microrods feature a hierar-chical architecture, designed for potential macromolecular payloads, and silica-based systems have previously been shown to successfully deliver oligonucleotides in vitro. However, current microrod systems mainly rely on nanoparticulate silica-based frameworks with limited biodegradibility and lack targeted disintegration under the acidic conditions encountered in phagolysosomes. Therefore, a nanostructured calcium phosphate framework is proposed as a biodegradable and resorbable alternative with pH-responsive characteristics. This study describes the fabrication of nanostructured, rod-shaped calcium phosphate microparticles and discusses their suitability as a po-tential pulmonary drug-delivery platform. The particles feature a dissolution-driven disintegration in acidic and ion-rich environments relevant to phagolysosomes. In ad-dition, the particles exhibited a favorable acute cytotoxicity profile in the murine alve-olar macrophage cell line MH-S compared with their SiO2-based counterpart. Com-parative RNA-seq analysis of MH-S that are exposed to the particles indicate a mild transcriptomic response, while canonical signatures of classical or alternative macro-phage activation programs were not observed, supporting a generally well-tolerated exposure profile of the carrier. Together, these findings establish key prerequisites for employing calcium phosphate microrods as a biodegradable pulmonary carrier plat-form in subsequent studies incorporating therapeutic cargo.</description><dates><publication>2026/05/14</publication></dates><accession>GSE317613</accession><cross_references><GSM>GSM9475309</GSM><GSM>GSM9475308</GSM><GSM>GSM9475307</GSM><GSM>GSM9475306</GSM><GSM>GSM9475305</GSM><GSM>GSM9475304</GSM><GSM>GSM9475315</GSM><GSM>GSM9475303</GSM><GSM>GSM9475314</GSM><GSM>GSM9475313</GSM><GSM>GSM9475302</GSM><GSM>GSM9475301</GSM><GSM>GSM9475312</GSM><GSM>GSM9475311</GSM><GSM>GSM9475310</GSM><GPL>34475</GPL><GSE>317613</GSE><taxon>Mus musculus</taxon><PMID>[42076080]</PMID></cross_references></HashMap>