# Breaking Barriers: Advancements in CNS Drug Delivery for Glioblastoma

**Authors:** Nicole Al Fidawi, Cecile Z. Attieh, Lara Baghdadi, Chahine El Bekai, Safaa Sayadi, Ghassan Nabbout, François Sahyoun, Hilda E. Ghadieh, Sami Azar, Frederic Harb

PMC · DOI: 10.3390/medsci14010073 · Medical Sciences · 2026-02-05

## TL;DR

This paper discusses new methods to deliver drugs to treat glioblastoma, a deadly brain tumor, by overcoming the blood-brain barrier and improving treatment effectiveness.

## Contribution

The paper highlights novel drug delivery systems and their potential to improve glioblastoma treatment outcomes.

## Key findings

- Nanoparticle-mediated delivery and focused ultrasound can transiently disrupt the blood-brain barrier for drug delivery.
- Convection-enhanced infusion and implantable devices show promise in increasing local drug exposure and reducing toxicity.
- Current challenges include ensuring safety and translating these methods into effective clinical therapies.

## Abstract

Glioblastoma is known as the most aggressive primary brain tumor in adults, and it is still largely not curable, with a median survival of approximately 15 months when standard multimodal therapy is applied. The standard treatment nowadays is maximal safe surgical resection, associated with radiotherapy and temozolomide. Treatment effectiveness is limited not only by an impassable blood–brain barrier (BBB) to drug delivery to the brain, but also by the heterogeneity of the tumors and intrinsic or acquired drug resistance, resulting in a certain and inescapable tumor relapse. Therefore, novel drug delivery systems are being designed to overcome the BBB and improve therapeutic efficacy. These approaches include nanoparticle-mediated delivery systems, convection-enhanced intra-tumoral infusion, implantable drug-releasing devices, and noninvasive focused ultrasound technology, which induced transient disruption of the BBB. These approaches are designed to enhance local drug exposure and reduce systemic toxicity with promising preclinical and early clinical results. However, many clinical and technical challenges remain, especially the need for safety, homogeneous drug delivery, and translation of these advances into effective clinical therapies. Current glioblastoma treatment landscape and opportunities include maturing delivery systems, novel therapeutic approaches, including targeted molecular therapies and immunotherapy, as well as personalized regimens. This multidisciplinary modality may have the capacity to help not only patients with GBM but others as well through a multimodal approach of targeted drug delivery and innovative therapy in the long run to improve clinical outcomes of GBM in patients.

## Linked entities

- **Chemicals:** temozolomide (PubChem CID 5394)
- **Diseases:** glioblastoma (MONDO:0018177)

## Full-text entities

- **Genes:** ABCB1 (ATP binding cassette subfamily B member 1) [NCBI Gene 5243] {aka ABC20, CD243, CLCS, ENPAT, GP170, MDR1}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, SLTM (SAFB like transcription modulator) [NCBI Gene 79811] {aka Met}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, LDLR (low density lipoprotein receptor) [NCBI Gene 3949] {aka LDLCQ2}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, ABCG2 (ATP binding cassette subfamily G member 2 (JR blood group)) [NCBI Gene 9429] {aka ABC15, ABCP, BCRP, BMDP, CD338, CDw338}, CXADRP1 (CXADR pseudogene 1) [NCBI Gene 653108] {aka CAR, CXADRP}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, IL4R (interleukin 4 receptor) [NCBI Gene 3566] {aka CD124, IL-4RA, IL4RA}, IL13RA2 (interleukin 13 receptor subunit alpha 2) [NCBI Gene 3598] {aka CD213A2, CT19, IL-13R, IL13BP}, SPATA2 (spermatogenesis associated 2) [NCBI Gene 9825] {aka PD1, PPP1R145, tamo}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, TF (transferrin) [NCBI Gene 7018] {aka HEL-S-71p, PRO1557, PRO2086, TFQTL1}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}
- **Diseases:** necrosis (MESH:D009336), Seizures (MESH:D012640), brain tumor (MESH:D001932), hypoxia (MESH:D000860), GBM (MESH:D005909), HNSCC (MESH:D000077195), neurological deterioration (MESH:D009422), disorders (MESH:D009358), nausea (MESH:D009325), bleeding (MESH:D006470), cerebral edema (MESH:D001929), intracranial hypertension (MESH:D019586), tumor IL-13 receptor (MESH:D018344), fatigue (MESH:D005221), thromboembolic (MESH:D013923), cancers (MESH:D009369), chromosomal abnormalities (MESH:D002869), AD (MESH:D000544), infection (MESH:D007239), edema (MESH:D004487), meningitis (MESH:D008580), cytotoxic (MESH:D064420), GBM (MESH:D005910), epileptic (MESH:D004827), metastasis (MESH:D009362), injury to (MESH:D014947), inflammation (MESH:D007249), brain disorders (MESH:D001927), carcinogenic (MESH:D011230)
- **Chemicals:** AgCl (MESH:C037548), Bleomycin (MESH:D001761), Nivolumab (MESH:D000077594), Ag (MESH:D012834), lapatinib (MESH:D000077341), docetaxel (MESH:D000077143), Bevacizumab (MESH:D000068258), Erlotinib (MESH:D000069347), cediranib (MESH:C500926), gadolinium (MESH:D005682), ATP (MESH:D000255), 5-ALA (MESH:C000614854), lomustine (MESH:D008130), lipid (MESH:D008055), gefitinib (MESH:D000077156), paclitaxel (MESH:D017239), irinotecan (MESH:D000077146), TMZ (MESH:D000077204), polymer (MESH:D011108), polyanhydride (MESH:D049388), cetuximab (MESH:D000068818), curcumin (MESH:D003474), gold (MESH:D006046), carmustine (MESH:D002330), Cisplatin (MESH:D002945), metal (MESH:D008670), AlCIPc (-), silica (MESH:D012822), doxorubicin (MESH:D004317), Gliadel (MESH:C574855)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** U87MG — Homo sapiens (Human), Glioblastoma, Cancer cell line (CVCL_0022), GBM02 — Homo sapiens (Human), Glioblastoma, Cancer cell line (CVCL_DG57)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12922005/full.md

## References

62 references — full list in the complete paper: https://tomesphere.com/paper/PMC12922005/full.md

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Source: https://tomesphere.com/paper/PMC12922005