Back to Search Start Over

Intratracheal Administration of Hyaluronan-Cisplatin Conjugate Nanoparticles Significantly Attenuates Lung Cancer Growth in Mice.

Authors :
Ishiguro S
Cai S
Uppalapati D
Turner K
Zhang T
Forrest WC
Forrest ML
Tamura M
Source :
Pharmaceutical research [Pharm Res] 2016 Oct; Vol. 33 (10), pp. 2517-29. Date of Electronic Publication: 2016 Jun 22.
Publication Year :
2016

Abstract

Purpose: To determine aerosol administration capability and therapeutic efficacy of the new formulation of hyaluronan cisplatin conjugates, HylaPlat™ (HA-Pt), for lung cancer treatment.<br />Methods: In vitro formulation stability test, 2D and 3D spheroid cell culture and in vivo efficacy studies using mouse orthotopic allograft models were conducted.<br />Results: The HA-Pt effectively attenuated cell growth in 2D and 3D cultures with IC50 of 2.62 and 5.36 μM, respectively, which were comparable to those with unconjugated control cisplatin-dependent growth inhibition (IC50 1.64 and 4.63 μM, respectively). A single dose of either 7.5 or 15 mg/kg HA-Pt (cisplatin equivalent) by intratracheal aerosol spray 7 days after Lewis lung carcinoma (LLC) cell inoculation markedly inhibited growth of LLC allografts in mouse lungs and resulted in a 90 or 94% reduction of tumor nodule numbers, respectively, as compared to those from the PBS control. Cancer stem cells and cisplatin resistant cells marker, CD44 expression decreased in the tumor nodules of the HA-Pt but not in those of cisplatin treated groups.<br />Conclusions: The current study suggests that an intratracheal aerosol administration of the HA-Pt nanoparticles offers an effective strategy for lung cancer treatment and this treatment may induce only limited cisplatin resistance.<br />Competing Interests: of any potential Conflicts of Interest: M.L. Forrest, W.C. Forrest, S. Cai and T. Zhang are employees and/or have ownership interest in HylaPharm, which has licensed HylaPlat technologies from the University of Kansas. No potential conflicts of interest were disclosed by the other authors.

Details

Language :
English
ISSN :
1573-904X
Volume :
33
Issue :
10
Database :
MEDLINE
Journal :
Pharmaceutical research
Publication Type :
Academic Journal
Accession number :
27335023
Full Text :
https://doi.org/10.1007/s11095-016-1976-3