PET imaging of distinct brain uptake of a nanobody and similarly-sized PAMAM dendrimers after intra-arterial administration

IntroductionWe have recently shown that intracerebral delivery of an anti-VEGF monoclonal antibody bevacizumab using an intra-arterial (IA) infusion is more effective than intravenous administration. While antibodies are quickly emerging as therapeutics, their disadvantages such as large size, production logistics and immunogenicity motivate search for alternatives. Thus we have studied brain uptake of nanobodies and polyamidoamine (PAMAM) dendrimers.MethodsNanobodies were conjugated with deferoxamine (DFO) to generate NB(DFO)(2). Generation-4 PAMAM dendrimers were conjugated with DFO, and subsequently primary amines were capped with butane-1,2-diol functionalities to generate G4(DFO)(3)(Bdiol)(110). Resulting conjugates were radiolabeled with zirconium-89. Brain uptake of (ZrNB)-Zr-89(DFO)(2) and (89)ZrG4(DFO)(3)(Bdiol)(110) upon carotid artery vs tail vein infusions with intact BBB or osmotic blood-brain barrier opening (OBBBO) with mannitol in mice was monitored by dynamic positron emission tomography (PET) over 30min to assess brain uptake and clearance, followed by whole-body PET-CT (computed tomography) imaging at 1h and 24h post-infusion (pi). Imaging results were subsequently validated by ex-vivo biodistribution.ResultsIntravenous administration of (ZrNB)-Zr-89(DFO)(2) and (89)ZrG4(DFO)(3)(Bdiol)(110) resulted in their negligible brain accumulation regardless of BBB status and timing of OBBBO. Intra-arterial (IA) administration of (ZrNB)-Zr-89(DFO)(2) dramatically increased its brain uptake, which was further potentiated with prior OBBBO. Half of the initial brain uptake was retained after 24h. In contrast, IA infusion of (89)ZrG4(DFO)(3)(Bdiol)(110) resulted in poor initial accumulation in the brain, with complete clearance within 1h of administration. Ex-vivo biodistribution results reflected those on PET-CT.ConclusionsIA delivery of nanobodies might be an attractive therapeutic platform for CNS disorders where prolonged intracranial retention is necessary.