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Evaluation of the clearance characteristics of liposomes in the human nose by gamma-scintigraphy

JaafariG Mahmoud Reza نويسنده , Tafaghodi Mohsen نويسنده , Sajadi Tabassi Seyed Abolghasem نويسنده

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The nasal cavity possesses many advantages as a site for drug delivery, such as, ease of administration, applicability for long term treatments and a large surface area for absorption. One important limiting factor for nasal drug delivery is the limited time available for absorption within the nasal cavity due to mucociliary clearance, Several drug delivery systems including different kinds of microspheres and liposomes have been tried for encapsulation of drugs and increasing the residence time in nasal cavity. In this study the clearance rate of three kinds of liposomes: neutral [phosphatidylcholin (PC) and cholesterol (Chol)], cationic (PC, Chol and stearylamine) and fusogenic (PC, Chol, dioleoylphosphatidylethanolamine) was determined by gamma scintigraphy with lactose powder being used as negative control. Liposomes were prepared by dehydration-rehydration method. 99mTc labeled liposomes were prepared using technetium pertechnetate in the presence of a potent reducing agent, stannus chloride, The labeling procedure was set in a manner that each 150 ~I of liposome suspensions contained 2 MBq of radioactivity. Labeling efficiency was calculated by paper chromatography using acetone as mobile phase. Each delivery system containing 2 MBq of activity was sprayed into right nostril of four healthy volunteers and one-minute static views were repeated each half hour until 4 hours. Clearance rates were compared using two Regions of Interest (ROls); the initial site of deposition of particles, and all of nasopharynx region. The clearance rate of each one of Iiposomes was calculated after applying the physical decay corrections, The mean labeling efficiencies for neutral, cationic and fusogenic liposomes were calculated as 91%, 20% and 69%, respectively. The cleared percent of preparations from nasopharynx region after 4 hours was determined as follows: neutralliposomes l8±2.9%; fusogenic liposomes 53.5± 1.2%; cationic liposomes 69.7±4.2%; lactose powder 74.5±4.9%. Neutral Iiposomes showed the lowest clearance rate compared to lactose powder (P