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In vivo retention and clearance kinetics of DiR-labeled AdMSC spheroids after injection into mouse salivary glands. (a) DiR-labeled AdMSC spheroids or spheroid + GC (untreated, spheroid, spheroid + GC 5% w/v, spheroid + GC 7% w/v) were injected into the IR-damaged mouse salivary gland, and their fluorescence signals were monitored by <t>IVIS</t> from days 1 to 28 until no detectable signal remained. (b) Quantification of the average radiant efficiency in the salivary gland region over time. (c) At day 28 post-injection, major organs (heart, liver, spleen, kidneys, lungs, and stomach) were harvested and imaged by IVIS to assess DiR signals. Data are presented as mean ± SD (n = 3 or n = 4). Statistical analysis was performed using one-way ANOVA followed by Tukey's post-hoc test. ns P > 0.05, ∗ P ≤ 0.05, ∗∗ P ≤ 0.01, and ∗∗∗ P ≤ 0.001.
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In vivo retention and clearance kinetics of DiR-labeled AdMSC spheroids after injection into mouse salivary glands. (a) DiR-labeled AdMSC spheroids or spheroid + GC (untreated, spheroid, spheroid + GC 5% w/v, spheroid + GC 7% w/v) were injected into the IR-damaged mouse salivary gland, and their fluorescence signals were monitored by <t>IVIS</t> from days 1 to 28 until no detectable signal remained. (b) Quantification of the average radiant efficiency in the salivary gland region over time. (c) At day 28 post-injection, major organs (heart, liver, spleen, kidneys, lungs, and stomach) were harvested and imaged by IVIS to assess DiR signals. Data are presented as mean ± SD (n = 3 or n = 4). Statistical analysis was performed using one-way ANOVA followed by Tukey's post-hoc test. ns P > 0.05, ∗ P ≤ 0.05, ∗∗ P ≤ 0.01, and ∗∗∗ P ≤ 0.001.
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Image Search Results


In vivo retention and clearance kinetics of DiR-labeled AdMSC spheroids after injection into mouse salivary glands. (a) DiR-labeled AdMSC spheroids or spheroid + GC (untreated, spheroid, spheroid + GC 5% w/v, spheroid + GC 7% w/v) were injected into the IR-damaged mouse salivary gland, and their fluorescence signals were monitored by IVIS from days 1 to 28 until no detectable signal remained. (b) Quantification of the average radiant efficiency in the salivary gland region over time. (c) At day 28 post-injection, major organs (heart, liver, spleen, kidneys, lungs, and stomach) were harvested and imaged by IVIS to assess DiR signals. Data are presented as mean ± SD (n = 3 or n = 4). Statistical analysis was performed using one-way ANOVA followed by Tukey's post-hoc test. ns P > 0.05, ∗ P ≤ 0.05, ∗∗ P ≤ 0.01, and ∗∗∗ P ≤ 0.001.

Journal: Bioactive Materials

Article Title: AdMSC spheroids encapsulating antioxidant hybrid protein carrier for irradiation-damaged salivary gland repair

doi: 10.1016/j.bioactmat.2026.03.049

Figure Lengend Snippet: In vivo retention and clearance kinetics of DiR-labeled AdMSC spheroids after injection into mouse salivary glands. (a) DiR-labeled AdMSC spheroids or spheroid + GC (untreated, spheroid, spheroid + GC 5% w/v, spheroid + GC 7% w/v) were injected into the IR-damaged mouse salivary gland, and their fluorescence signals were monitored by IVIS from days 1 to 28 until no detectable signal remained. (b) Quantification of the average radiant efficiency in the salivary gland region over time. (c) At day 28 post-injection, major organs (heart, liver, spleen, kidneys, lungs, and stomach) were harvested and imaged by IVIS to assess DiR signals. Data are presented as mean ± SD (n = 3 or n = 4). Statistical analysis was performed using one-way ANOVA followed by Tukey's post-hoc test. ns P > 0.05, ∗ P ≤ 0.05, ∗∗ P ≤ 0.01, and ∗∗∗ P ≤ 0.001.

Article Snippet: For in vivo fluorescence imaging, mice were anesthetized and scanned using an IVIS imaging system (IVIS Lumina S5, PerkinElmer) at predetermined time points (1, 3, 5, 7, 10, 14, 21, and 28 days) with excitation/emission settings appropriate for DiR (typically Ex 748 nm/Em 780 nm).

Techniques: In Vivo, Labeling, Injection, Fluorescence

Pharmacokinetics of 25% w/w CBD-loaded Pluronic® F127 polymeric micelles in ASD-like rats. (A) IVIS fluorescence micrographs of rat brains at different time points after i.n. administration of NIR-797-labeled CBD-loaded polymeric micelles, as imaged by IVIS (n = 4). (B) Fluorescence radiance intensity profiles in the brain of rat (n = 4). (C) IVIS fluorescence micrographs of rat olfactory bulbs 90 min after i.n. administration of NIR-797-labeled CBD-loaded polymeric micelles, as imaged by IVIS (n = 4). (D) CBD concentration in rat brains following the i.n. and oral administration of 25% w/w CBD-loaded Pluronic® F127 polymeric micelles and i.n. administration of CBD dissolved in propylene glycol. (E) CBD concentration in rat plasma following the i.n. and oral administration of 25% w/w CBD-loaded Pluronic® F127 polymeric micelles and i.n. administration of CBD dissolved in propylene glycol. In all the PK studies, the i.n. and oral CBD dose was 5 and 15 mg/kg, respectively. All data are presented as mean ± S.E. (n = 4).

Journal: Bioactive Materials

Article Title: Nose-to-brain administration of cannabidiol-loaded polymeric micelles improves the core behavioral symptoms of autism spectrum disorder

doi: 10.1016/j.bioactmat.2026.03.019

Figure Lengend Snippet: Pharmacokinetics of 25% w/w CBD-loaded Pluronic® F127 polymeric micelles in ASD-like rats. (A) IVIS fluorescence micrographs of rat brains at different time points after i.n. administration of NIR-797-labeled CBD-loaded polymeric micelles, as imaged by IVIS (n = 4). (B) Fluorescence radiance intensity profiles in the brain of rat (n = 4). (C) IVIS fluorescence micrographs of rat olfactory bulbs 90 min after i.n. administration of NIR-797-labeled CBD-loaded polymeric micelles, as imaged by IVIS (n = 4). (D) CBD concentration in rat brains following the i.n. and oral administration of 25% w/w CBD-loaded Pluronic® F127 polymeric micelles and i.n. administration of CBD dissolved in propylene glycol. (E) CBD concentration in rat plasma following the i.n. and oral administration of 25% w/w CBD-loaded Pluronic® F127 polymeric micelles and i.n. administration of CBD dissolved in propylene glycol. In all the PK studies, the i.n. and oral CBD dose was 5 and 15 mg/kg, respectively. All data are presented as mean ± S.E. (n = 4).

Article Snippet: Imaging was performed using an IVIS® Spectrum CT system from PerkinElmer (Waltham, MA, USA).

Techniques: Drug discovery, Fluorescence, Labeling, Olfactory, Concentration Assay, Clinical Proteomics