The Influence of Size on the Intracranial Distribution of Biomedical Nanoparticles Administered by Convection-enhanced Delivery in Minipigs

• Published in: ACS nano 2024-07, Vol.18 (27), p.17869-17881
• Main Authors: Amirrashedi, Mahsa, Jensen, Andreas Ingemann, Tang, Qing, Straathof, Natan Johannes Willem, Ravn, Katharina, Pedersen, Christian G.T., Langhorn, Louise, Poulsen, Frantz Rom, Woolley, Max, Johnson, David, Williams, Julia, Kidd, Charlotte, Thisgaard, Helge, Halle, Bo
• Format: Article
• Language: English
• Subjects: Animals; Blood-Brain Barrier - metabolism; Brain - diagnostic imaging; Brain - metabolism; Convection; Copper Radioisotopes - chemistry; Drug Delivery Systems; Gold - chemistry; Liposomes - chemistry; Metal Nanoparticles - chemistry; Nanoparticles - chemistry; Particle Size; Polyethylene Glycols - chemistry; Positron-Emission Tomography; Swine; Swine, Miniature
• ISSN: 1936-0851; 1936-086X; 1936-086X
• DOI: 10.1021/acsnano.4c04159

Because of the blood–brain barrier (BBB), successful drug delivery to the brain has long been a key objective for the medical community, calling for pioneering technologies to overcome this challenge. Convection-enhanced delivery (CED), a form of direct intraparenchymal microinfusion, shows promise but requires optimal infusate design and real-time distribution monitoring. The size of the infused substances appears to be especially critical, with current knowledge being limited. Herein, we examined the intracranial administration of polyethylene glycol (PEG)-coated nanoparticles (NPs) of various sizes using CED in groups of healthy minipigs (n = 3). We employed stealth liposomes (LIPs, 130 nm) and two gold nanoparticle designs (AuNPs) of different diameters (8 and 40 nm). All were labeled with copper-64 for quantitative and real-time monitoring of the infusion via positron emission tomography (PET). NPs were infused via two catheters inserted bilaterally in the putaminal regions of the animals. Our results suggest CED with NPs holds promise for precise brain drug delivery, with larger LIPs exhibiting superior distribution volumes and intracranial retention over smaller AuNPs. PET imaging alongside CED enabled dynamic visualization of the process, target coverage, timely detection of suboptimal infusion, and quantification of distribution volumes and concentration gradients. These findings may augment the therapeutic efficacy of the delivery procedure while mitigating unwarranted side effects associated with nonvisually monitored delivery approaches. This is of vital importance, especially for chronic intermittent infusions through implanted catheters, as this information enables informed decisions for modulating targeted infusion volumes on a catheter-by-catheter, patient-by-patient basis.