The 3<sup>rd</sup> International Conference on Drug Discovery & Therapy: Dubai, February 7 - 11, 2011
Drug Delivery & Targeting (Discovery)

Many biologically active molecules are very active in vitro, but never reach the clinic because of lack of absorption and/or poor in vivo stability. Although a range of delivery systems is available, the delivery of sensitive drugs such as peptides, nucleic acid based therapeutics (including antisense DNA and siRNA), simple and complex carbohydrates, and synthetic vaccines presents a major challenge to the pharmaceutical industry. Industry experts agree that approximately 10% of the costs of drug development program should be allocated to aspects of drug delivery. New developments in drug delivery research are likely to have enormous economic impacts upon the pharmaceutical and biotechnology industries. In fact, drug delivery research represents a US$70 billion a year industry. Centres for Drug Delivery have been established all over the world to promote research, development and training in drug delivery science. There has also been a focus on realizing the commercial potential of innovative molecules (e.g. peptides, nucleic acid based therapies and vaccines) or delivery technologies that are developed from the centres’ research. Research in drug delivery is multidisciplinary, requiring knowledge of how drugs work, their chemical and physical properties, how these properties affect the drugs in vivo behaviour, and what could be done to potentially solve any delivery problems associated with drug molecules. Therefore, drug delivery research necessitates interdisciplinary collaborations both at a national and international level.

Drug Delivery & Targeting (Therapy)

Currently, there are no drugs supported by sufficient evidence of efficacy for cerebral vasospasm in patients with subarachnoid hemorrhage, despite abundant evidence of anti-vasospasm drugs at an experimental level. We have developed a drug-delivery system using a vasodilating drug that can be implanted intracranially at the time of surgery for aneurysm clipping, without systemic side effects or side effects associated with long-term intrathecal drug administration through indwelling catheters.

We started our project in 1994 for making slowly-releasing drug-delivery system in vitro, because cerebral vasospasm occurs 4-14 days following subarachnoid hemorrhage. A rod-shaped pellet (1 mm in diameter, 10 mm in length, containing 1 mg of nicardipine) for animal study was prepared by heat compression. Release curve from the pellets was adjusted similar to the time course of cerebral vasospasm by changing the combination of molecular weight and lactic acid ratio of Copoly (lactic/glycolic acid) and nicardipine. We presented the efficacy and safety of this drug delivery system using both canine double hemorrhage and clot placement model. The mean concentration of nicardipine in the clots was 1.5x10-4 mol/L on Day 7 and 5.1x10-6 on Day 14. This drug delivery system can prevent vasospasm significantly in dogs, while maintaining an appropriate concentration of nicardipine in the clot adjacent to the arteries, since maximal relaxation is achieved by 10-6 mol/L of nicardipine. Since October 1999, nicardipine pellets (NPs) (2 mm in diameter, 10 mm in length, containing 4 mg of nicardipine) have been used to prevent vasospasm in patients with SAH. The study was approved by the University Ethical Committee, and informed consent was obtained. A frontotemporal craniotomy and a midline frontal craniotomy (pterional and anterior interhemispheric approach) were performed for aneurysms in the internal carotid artery (ICA), middle cerebral artery (MCA), basilar artery, anterior communicating artery, and distal anterior cerebral artery (ACA). NPs were placed in the cistern of the ICA, the MCA, and/or the ACA, where thick clots existed, and, therefore, vasospasm related to delayed ischemic neurological deficits (DIND) was highly probable. The number of pellets and the location of the placement depended on the amount and site of the subarachnoid clot in the preoperative CT scans, the operative field, and the craniotomy. Cerebral vasospasm was assessed by DIND, and angiography was performed in all patients on Days 7 to 12. We published a preliminary report on the efficacy and safety of NPs to prevent vasospasm in 20 SAH patients. Vasospasm was completely prevented in the arteries in cisterns with thick clots, where vasospasm was highly expected, by placing NPs adjacent to the arteries during surgery. In the first 100 patients treated with NPs, the ratio of DIND, severe angiographical vasospasm and cerebral infarctions was 7%, 11%, and 5%, respectively. No complications were experienced. Thirty-two patients with severe SAH and undergoing aneurysm clipping were included in the single center, randomized, double-blind trial in Germany. The incidence of angiographic vasospasm in proximal vessel segments was significantly reduced after implantation of NPs (73% control versus 7% NPs). Significant differences occurred also for the majority of distal vessel segments. Computed tomography scans revealed a lower incidence of delayed ischemic lesions (47% control versus 14% NPs). The NPs group demonstrated more favorable modified Rankin and National Institute of Health Stroke scales as well as a significantly lower incidence of deaths (38% control versus 6% NPs).

We found that vasospasm is completely prevented in arteries in cisterns with thick clots, where vasospasm is highly expected, by placing NPs adjacent to the arteries during surgery. Lesser efficacy was found for arteries remote from the placement of pellets. Implantation of NPs improves clinical outcome of SAH patients. We consider that this could not be achieved by developing new drugs but by developing methods to maintain an appropriate concentration of the drug in the target cerebral artery and its surrounding environment.