Fiber-optic triggered release of liposome in vivo: implication of personalized chemotherapy

International Journal of Nanomedicine, Aug 2015

Fiber-optic triggered release of liposome in vivo: implication of personalized chemotherapy Huei-Ling Huang,1 Pei-Hsuan Lu,1 Hung-Chih Yang,1 Gi-Da Lee,1,2 Han-Ru Li,1 Kuo-Chih Liao1 1Graduate Institute of Biomedical Engineering, National Chung Hsing University, 2Department of Radiology, Taichung Veterans General Hospital, Taichung, Taiwan Abstract: The aim of this research is to provide proof of principle by applying the fiber-optic triggered release of photo-thermally responsive liposomes embedded with gold nanoparticles (AuNPs) using a 200 µm fiber with 65 mW and 532 nm excitation for topical release in vivo. The tunable delivery function can be paired with an apoptosis biosensor based on the same fiber-optic configuration for providing real-time evaluation of chemotherapy efficacy in vivo to perform as a personalized chemotherapy system. The pattern of topical release triggered by laser excitation conveyed through optical fibers was monitored by the increase in fluorescence resulting from the dilution of self-quenching (75 mM) fluorescein encapsulated in liposomes. In in vitro studies (in 37°C phosphate buffer saline), the AuNP-embedded liposomes showed a more efficient triggered release (74.53%±1.63% in 40 minutes) than traditional temperature-responsive liposomes without AuNPs (14.53%±3.17%) or AuNP-liposomes without excitation (21.92%±2.08%) by spectroscopic measurements. Using the mouse xenograft studies, we first demonstrated that the encapsulation of fluorescein in liposomes resulted in a more substantial content retention (81%) in the tumor than for free fluorophores (14%) at 120 minutes after administration from in vivo fluorescence imaging. Furthermore, the preliminary results also suggested the tunable release capability of the system by demonstrating consecutive triggered releases with fiber-optic guided laser excitation. Keywords: fiber-optic guided excitation, light excitation triggered release, photo-thermal responsive liposome, gold nanoparticles, tunable release in vivo

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Fiber-optic triggered release of liposome in vivo: implication of personalized chemotherapy

International Journal of Nanomedicine Fiber-optic triggered release of liposome in vivo: implication of personalized chemotherapy 0 Department of radiology, Taichung Veterans general hospital , Taichung , Taiwan 1 g raduate Institute of Biomedical engineering, National chung hsing University The aim of this research is to provide proof of principle by applying the fiber-optic triggered release of photo-thermally responsive liposomes embedded with gold nanoparticles (AuNPs) using a 200 μm fiber with 65 mW and 532 nm excitation for topical release in vivo. The tunable delivery function can be paired with an apoptosis biosensor based on the same fiber-optic configuration for providing real-time evaluation of chemotherapy efficacy in vivo to perform as a personalized chemotherapy system. The pattern of topical release triggered by laser excitation conveyed through optical fibers was monitored by the increase in fluorescence resulting from the dilution of self-quenching (75 mM) fluorescein encapsulated in liposomes. In in vitro studies (in 37°C phosphate buffer saline), the AuNP-embedded liposomes showed a more efficient triggered release (74.53%±1.63% in 40 minutes) than traditional temperatureresponsive liposomes without AuNPs (14.53%±3.17%) or AuNP-liposomes without excitation (21.92%±2.08%) by spectroscopic measurements. Using the mouse xenograft studies, we first demonstrated that the encapsulation of fluorescein in liposomes resulted in a more substantial content retention (81%) in the tumor than for free fluorophores (14%) at 120 minutes after administration from in vivo fluorescence imaging. Furthermore, the preliminary results also suggested the tunable release capability of the system by demonstrating consecutive triggered releases with fiber-optic guided laser excitation. - huei-ling huang 1 Pei-hsuan lu 1 hung-chih Yang 1 gi-Da lee 1,2 han-ru li 1 Kuo-chih liao 1 Liposomes are by far the most successful drug delivery vehicle in commercialization for clinical applications.10 For chemotherapy, the targeting (active or passive) and longlasting content release characteristics of liposome vesicles can facilitate the accumulation of a higher concentration/ percentage of the drug in the tumor (ie, increase the therapeutic index) and prevent the drug (toxic agent) from being exposed to normal tissues, which could cause lateral damage during transportation or allow it to be destroyed before arriving at the target tumor site. Liposome-delivered anticancer agents, such as doxorubicin, have been proved to reduce side effects (cardiotoxicity, gastrointestinal toxicity, stomatitis, hair loss, etc) while exhibiting superior performance or preserving efficacy in clinical studies and maintaining an extended period of therapeutic concentration.11–13 Considerable efforts have been devoted to extend the lifetime and integrity of liposomes in the bloodstream to periods on the order of days, raising the successful rate of transportation to 8 1 0 2 l u J 2 1 n o 7 5 1 . 9 2 1 . 6 9 1 . 5 y b / m o c . s s e r p e v .do l.y //www seon tphaesstiavregedtr ulogcraetlieoans,1e4,e15ffbicuitetnhceyluippoosnoamrreisviinngtearftetrheewdeitshtitnhae:s lu ttph aon tion and reduce clinical efficacy.16–19 An active triggered rom rspe mechanism is required to facilitate sufficient liposome fded roF content release in situ for optimal treatment effects,16–21 and loa a non-invasive or minimally invasive monitoring method is onw required to adjust the topical release kinetics tailored for each nde subject in vivo by detecting drug-induced bio-events, with iicd the goal of achieving and extending the therapeutic dosage oem period without exceeding toxic levels.22–24 naN The conventional liposome triggered-release systems lfao in development can be divided into external (remote) and run internal (intrinsic) triggers.16,21 Internal triggers are designed lJoa to compromise liposome membrane integrity using bioitno transformable components resulting from elevated enzyme trane expression (phosphatase in prostatic carcinoma tissue or In phospholipase A2 in breast or pancreatic cancer) or biophysical changes (endocytosed liposomes degraded by the endosomal pathway upon dropping pH from 6.5 to 4) at disease sites. External triggers convey external energy (ultrasound, heatgenerating light, microwaves or alternative magnetic fields) through tissues to focus on the target disease site and crush the accumulated liposomes in situ. However, both systems suffer from the inconsistency of subjects caused by in vivo fluctuations. Internal trigger systems could experience limited efficiency or delayed release due to highly variable in vivo biophysical changes (pH, temperature, or chemical reactions competing with enzyme activity) and problematic specificity (phospholipase expressed not only in cancerous tissue but also in inflammation tissue).21 The energy input of external submit your manuscript | www.dovepress.com Dovepress trigger systems could be significantly attenuated, reflected, and scattered during propagation through highly inhomogeneous and subject-dependent sophisticated bio-media, preventing it from attaining sufficient and consistent penetration in different subjects for clinical uses.16 The disadvantages of both conventional trigger methods are evidenced by the small number of animal studies demonstrating trigger release kinetics in vivo and the limited success in achieving adequate responses in vivo (for example, heat-generating methods cannot produce a uniform temperature increase in tumors with a diameter 1 cm).17,18,25–27 In addition, the release profiles of most triggers in development (internal and external) may be controversial because they are expected to rupture liposomes and cause a burst discharge.16,21 However, an ideal drug delivery system should steadily maintain the released therapeutic dosage (subject-dependent) for an extended period and prevent excess therapeutic agents (those which could not be absorbed by target cells or tissues) from diffusing out of the target site and resulting in lateral damage on exposed non-target tissue. Our research group is developing a percutaneous sensing and therapeutic platform with a probe composed of hair-sized fiber bundles.22–24,28,29 The probe can comprise optical fibers for conveying excitation light and detecting returning reflection or fluorescent emission, as well as microcapillaries for delivering biomarker diagnosing agents or therapeutic agents in batches or continuously by pneumatic pressure from a spritzer or mechanical pressure from a syringe pump. The first application is a personalized chemotherapy system with a tunable chemotherapy agent delivery function (Figure 1A) and an in vivo apoptosis monitoring sensing capability (Supplementary materials 1 and 2), both sharing the same fiber bundles for agent delivery and light transmission.22 The experimental chemotherapy agent delivery platform delivers photo-thermally responsive liposomes directly into tumor, instead of relying on systematic intravenous administration. Dickerson et al demonstrated in a mouse study that intratumoral injection was more efficient at accumulating drugs in tumor tissue than intravenous administration.4 The proposed delivery system for personalized chemotherapy may also eliminate the inconsistency issue of non-invasive irradiation from conventional light sources,30 which was demonstrated in the study. The hair-like dimension of the implantable probe enables conventional clinical imaging modalities such as guided needle insertion (a similar procedure to biopsy sampling) to be used to place the fiber bundle probe within reach of deeper tumors (Figure 1C). The aim of this research is to provide proof of principle by applying the fiber-optic triggered release of photo-thermally 8 1 0 2 l u J 2 1 n o 7 5 1 . 9 2 1 . 6 9 1 . 5 y b / m o c . s s e r p e v .do l.y //www seon :s lu tp a th on s rom rpe fded roF a o l n w o d e n ii c d e m o n a N f o l a n r u o J l a n o it a n tr e n I responsive liposomes for topical release in vivo (in tumors of xenograft mice, Figure 1B) using a 200 μm optical fiber and a 65 mW continuous wave (CW) diode laser (Figure 1A). The photo-thermally reactive liposomes consisted of hydrophobic gold nanoparticles (AuNPs) tethered to the membrane of a temperature-responsive liposome; this design was responsible for converting light energy into heat by surface plasma resonance to increase liposome permeability when reaching the phase transition temperature.16,21,31 AuNPs are well recognized as biocompatible and have been applied in medical studies for decades, and thermal responsive liposomes are under clinical trials, such as 1,2-dipalmitoyl-sn-glycero-3-phosphatidylcholine (DPPC)-based Thermodox in Phase III.32,33 The pattern of triggered content release was quantified by an increase in fluorescence (in vivo fluorescence imaging) due to the dilution of a 75 mM (self-quench concentration) fluorescein solution when released from the liposome (Figure 2).34 Experimental Materials All reagents and solvents were acquired from SigmaAldrich (St Louis, MO, USA) and used as received unless otherwise indicated. DPPC, 1-myristoyl-2-palmitoylsn-glycero-3-phosphotydilcholine (MPPC), 1,2-distearoyl-sn-glycero-3-phosphatidylcholine (DSPC), and 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N[methoxy (polyethylene glycol)-2000] (DSPE-PEG2k) were obtained from Avanti Polar Lipids (Alabaster, AL, USA) stored at −20°C in chloroform. Sephadex G-75 was obtained from GE Healthcare Life Science (Pittsburgh, PA, USA) and hydrated in deionized water at 4°C overnight before applied for gel filtration. synthesis and characterization of auNP The synthesis method was adapted from literature by singlephase reduction of gold trichloride.35 In brief, 7.5 mg AuCl3 dissolved in 1 mL didodecyldimethylammonium bromide was reduced by 25 mg tetrabutylammonium borohydride dissolved in 1 mL didodecyldimethylammonium bromide solution in the presence of 43 mg decanoic acid dissolved in 2.5 mL toluene under vigorous mixing overnight, then stabilized by adding 79 μL 0.5 M tri-n-octylphosphine in toluene at 60°C for 5 minutes. After cooling to room temperature, the AuNPs were recrystalized by dropwise addition of 300 μL //www seon :s lu tp a th on s rom rpe fded roF a o l n w o d e n ii c d e m o n a N f o l a n r u o J l a n o it a n tr e n I methanol and separated by centrifugation at 3,000 rpm for 5 minutes. The precipitated AuNPs were then dissolved in chloroform and characterized by absorption spectrum (Synergy™ Mx Multi-Mode Microplate Reader, Biotek, Winooski, VT, USA) with 1 cm pathlength Bio-Cell™ for confirmation of AuNPs existence with the surface plasma resonance peak. Particle size distribution of the AuNP/chloroform solutions was measured by dynamic laser scattering (DLS, Zetasizer Nano, Malvern Instruments, Malven, UK). AuNPs were deposited onto a carbon coated copper grid after evaporation of chloroform in air and inspected by high-resolution transmission electron microscopy (HR-TEM, JEM-2010, Jeol, Tokyo, Japan) with selected particle diameter calculated by Image J software (1.48v, NIH, Bethesda, MD, USA) when compared with scale bar on the images. AuNPs were deposited onto a glass slide after evaporation of chloroform in air and inspected by X-ray diffractometer (Bruker, Billerica, MA, USA) for lattice structure identification. Concentration of AuNP/chloroform solutions was determined by first estimating the extinction coefficient (ε) from the average core diameter (D) of AuNPs measured by HR-TEM with 5174 the formula: ln ε=3.32 ln D +10.8, and then calculated the concentration from the absorbance of surface plasma resonance peak (A) with the formula of Beer–Lambert law: A=ε×1 (pathlength of Bio-Cell™ in cm) × C (concentration in M) as literature.36 Photo-thermal conversion of auNP by fiber-optic guided laser excitation In all, 2 mL AuNPs solution in chloroform at different concentrations was loaded in 15×125 mm pyrex test tubes with silicone seal. The solution in each test tube was wrapped with aluminum foil and stimulated with 200 μm multi-mode optical fiber (FIBER-200-VIS, OceanOptics, Dunedin, FL, USA) guided 65 mW diode pumped solid-state laser (TWC Opto Corp, Taipei, Taiwan) with the emission end of the optical fiber was placed beneath the surface of the solution through the silicone seal and 2 cm above the bottom of the test tube (Figure 3A). A digital thermometer (GE-363D, Dr AV Technology Co. Ltd., Changhua, Taiwan) was also placed beneath the surface of the solution through the silicone seal about the same depth of the end of optical fiber to monitor 8 1 0 2 l u J 2 1 n o 7 5 1 . 9 2 1 . 6 9 1 . 5 y b / m o c . s s e r p e v .do l.y //www seon :s lu tp a th on s rom rpe fded roF a o l n w o d e n ii c d e m o n a N f o l a n r u o J l a n o it a n tr e n I the excitation time-dependent temperature changes of the solution under continuously excitation. Fabrication and characterization of photo-thermal responsive liposome The fabrication method was adapted from the literature by the lipid film hydration extrusion method.37 In brief, phospholipids or cholesterol (Chol) in chloroform were mixed in molar ratios 90:10:4 (DPPC:MPPC:DSPE-PEG2k) or 90:10 (DSPC:DPPC), or 80:20 (DPPC:Chol) for achieving a lipid concentration of 20 mg/mL with AuNP/chloroform concentrations ranged 0–132 ng/mL, dried into a thin film by convection of nitrogen and followed by vacuum overnight. The dried lipid/AuNPs film was rehydrated with isotonic 75 mM fluorescein solution under sonication at 55°C. The resultant liposomes were extruded gradually through 400, 200, and 100 nm polycarbonate membranes (21 times each) to form large unilamellar vesicles.38 The unencapsulated fluorescein was then removed by column filtration with Sephadex G-75 (GE Healthcare, Pittsburgh, PA, USA) applying isotonic saline as elute phase, and collected with lipid concentration at 5 mg/mL measured by phospholipid assay (Wako Chemicals USA, Inc, Richmond, VA, USA). The mean diameter of the liposomes was verified by DLS (Zetasizer Nano, Malvern Instruments) and TEM (JEM-1400, Jeol). In isotonic saline solutions, the liposomes were found to maintain their structural stability for up to 5 weeks when stored at 4°C with less than 0.1% payload leaking observed by fluorescence intensity when encapsulation with 75 mM (self-quench) fluorescein solution. Fiber-optic guided laser excitation triggered liposome release in vitro In all, 2 mL 75 mM fluorescein entrapped liposome solution with a lipid concentration of 5 mg/mL was loaded in a 15×125 mm pyrex test tube with silicone seal, wrapped with aluminum foil and pre-warmed to 37°C by immersing in water bath. The solution was stimulated with 200 μm multi-mode optical fiber (FIBER-200-VIS, OceanOptics) guided 65 mW diode pumped solid-state laser (TWC Opto Corp, Taoyuan, Taiwan) with the emission end of the optical fiber was placed beneath the surface of the solution and 2 cm above the bottom of the test tube (Figure 4A). The fibercoupled laser module had CW emission beam as circular spot //www seon :s lu tp a th on s rom rpe fded roF a o l n w o d e n ii c d e m o n a N f o l a n r u o J l a n o it a n tr e n I with ,5% power fluctuation, ,0.5 nm spectral line-width and coupled into optical fiber with SubMiniature version A type connector. The self-quenching property of fluorescein at a concentration of 75 mM was used to quantify the percent fluorophore release from liposome. Fluorescein fluorescence is self-quenched inside the liposomes, but the fluorescence quenching is relieved after its release from liposome (Figure 2).34 Aliquots of 50 μL liposome solution were sampled at different intervals during laser excitation, then mixed with 50 μL isotonic saline, loaded in wells of 96-well plate, and their fluorescent emission intensities were measured by end-point detection of microplate reader (Synergy™ Mx Multi-Mode Microplate Reader, Biotek) applying 488 nm as an excitation wavelength and 520 nm as an emission wavelength. The percent fluorophore release was determined by the following formula: [(It − Ii)/(Id − Ii)] ×100%, where It was the measured intensity at time t, Id was the signal measured after liposome destruction by mixing aliquots of 50 μL liposome solution with 50 μL detergent (30 mM n-octyl-β-D-glucopyranoside), and Ii was the measured initial fluorescence. Consecutive triggered release of the AuNP-liposomes was tested in saline or rat plasma. Rat plasma was collected from tail vein of Sprague-Dawley rats (aged 17–19 weeks, 225±22.7 g) purchased from BioLASCO Taiwan Co, LTD (Yilan, Taiwan) after allowed to clot for a minimum of 45 minutes, and centrifugation at 2,000 rpm for 10 minutes to separate blood cells approved by the Institution Animal Care and Use Committee (IACUC) of National Chung Hsing University (IACUC Approval No 101–109). Murine xenograft model Nu/nu nude mice (aged 7–9 weeks, 32.5±2.7 g), purchased from BioLASCO Taiwan Co, LTD, were maintained in Experimental Animal Center of National Chung Hsing University, and studied following procedures approved by the IACUC of National Chung Hsing University (IACUC Approval No 101–108). Two to three mice were housed to each cage in an individually ventilated, temperature 5176 8 1 0 2 l u J 2 1 n o 7 5 1 . 9 2 1 . 6 9 1 . 5 y b / m o c . s s e r p e v .do l.y //www seon :s lu tp a th on s rom rpe fded roF a o l n w o d e n ii c d e m o n a N f o l a n r u o J l a n o it a n tr e n I (23°C±2°C), and humidity (50%–55%) controlled facilities, on 12 hours light, 12 hours dark cycle, and had free access to sterilized laboratory chow and water. The human breast adenocarcinoma cell line, MDA-MB 231, was obtained from the National Health Research Institute Cell Bank (Hsinchu, Taiwan) and cultured as recommended by the American Type Culture Collection (Manassas, VA, USA) with culture reagents obtained from Quantum Biotechnology (distributor of Life Technologies, Inc. and Invitrogen, Taichung, Taiwan) unless otherwise indicated. The cell culture medium was Dulbecco Modified Eagle Medium (DMEM) with 10% fetal bovine serine (FBS). Approximately 1 mL mixtures (volume ratio =1:1) of phenol red-free matrigel matrix (Bertec Enterprise Co Ltd, distributor of BD Bioscience, Taichung, Taiwan) and culture medium (DMEM with 10% FBS) with the suspension of 1×107 MDA-MB 231 cells were injected subcutaneously into both dorsal flanks (the same level above the dorsal-ventral adjunction) of the mice to grow xenografts with minimal widths around 1 cm. The xenografts were allowed to develop for 5 weeks before characterization with in vivo imaging inspections. Fluorescent imaging in vivo The in vivo fluorescence images of the mice were acquired using a Xenogen IVIS® Imaging System 200 Series (Caliper Life Science/Xenogen, Alameda, CA, USA), which features a temperature-controlled, light-tight imaging chamber and a cryogenically cooled back-illuminated digital charge-coupled device camera. Before and during the examination periods, anesthesia of the mice was initiated and maintained using the inhalation of isoflurane in oxygen (1%–2.5% isoflurane) in the isolated chamber of the system. In all, 50 μL liposome solution prepared as mentioned above (section “Fabrication and characterization of photo-thermal responsive liposome”) was administrated directly into the center of tumors. Image acquisition and processing was accomplished with Living Image® Software V2.6 (Caliper Life Science/Xenogen) on a PCbased system. The mice were brought to the imaging chamber at several time points after dye injection, placed in the center of the field of view (deliberately chosen as 13 cm ×13 cm) with the aid of the green laser alignment projector grid, and scanned with an excitation passband at 445–490 nm, an emission passband at 515–575 nm, 3 seconds exposure time, medium binning, and 4 seconds f/stop. Both delineation of tumor boundary and calculation of normalized fluorescence at the tumor area on the in vivo fluorescent images were processed by programs coded in MATLAB R2013a software (The MathWork Inc, Natick, MA, USA). Results characterization of auNP The absorbance spectrum of the resultant dark-reddish chloroform solution (Figure 3B) had a well-defined surface plasma resonance band with a maximal absorbance at approximately 522 nm (Figure 5C), confirming the existence of AuNPs in the chloroform solution. Those hydrophobic AuNPs were spherical in shape and had a uniform particle size distribution around 3–7 nm, as observed with HR-TEM (Figure 5A). Further examination by DLS analysis suggested that the particle size ranged from 2 nm to 11 nm, mainly distributed from 3 nm to 7 nm with an average value of 5.55±2.1 nm, and had size distribution polydiversity index smaller than 0.079 (Figure 5B). The crystal lattice of the nanostructure was in face-centered cubic shape, as identified by the X-ray diffraction pattern with several lattice planes (1 1 1), (2 0 0), (2 2 0), (3 1 1), and (2 2 2) as shown in Figure 5D. Photo-thermal energy conversion efficiency of AuNPs in vitro To investigate the photo-thermal energy conversion efficiency of AuNPs, a fiber-optic guided 65 mW laser emitting at 532 nm (near the surface plasma resonance band of AuNPs at approximately 522 nm, Figure 5C) was used to stimulate 2 mL AuNPs in chloroform at several concentrations. The laser, upon exiting the internal end (beneath the surface of the solution) of the optical fiber, propagated as a collimating beam, penetrating the dark-reddish AuNP/chloroform solution at all concentrations examined in the study, and formed a circular spot on the bottom surface of the test tube as shown in Figure 3B. The temperature increases of the AuNP/chloroform solutions after laser stimulation were recorded at regular time intervals to indicate the efficiency of conversion. It was found that the photo-thermal conversion efficiency (temperature rise) was in proportion to the AuNP concentration and excitation duration when excitation light path (h) was fixed at 2 cm before reaching a plateau approximately 7–10 minutes after laser stimulation (Figure 3C). The excitation band of the green laser (532 nm) is far from the absorption band of the solvent, chloroform (at ,250 nm), which was reflected in the relatively insignificant temperature rise (0.2°C±0.51°C) of a solution without AuNPs. With AuNPs at 4.5×10−7 or 9×10−7 M, the solutions were heated at 3.9°C±0.15°C or 5.9°C±0.63°C, respectively. Fiber-optic guided laser triggered liposome release in vitro Three of the most common thermal responsive liposomes formula, 90:10:4 (DPPC:MPPC:DSPE-PEG2k) or 90:10 //www seon :s lu tp a th on s rom rpe fded roF a o l n w o d e n ii c d e m o n a N f o l a n r u o J l a n o it a n tr e n I (DSPC:DPPC), or 80:20 (DPPC:Chol), were tethered with AuNPs up to 132 ng/mL for exploring the optimal photoresponsive liposome for the fiber-optic guided laser triggered release study.17,26,27,39–42 The 90:10:4 (DPPC:MPPC:DSPEPEG2k) liposome with 33 ng/mL AuNPs achieved the strongest photo-thermal conversion efficiency while maintaining decent liposome integrity at physiological temperature without causing significant leakage (21.92%±2.08% in 40 minutes without excitation) as shown in Figure 6. The AuNP-incorporated liposomes were spherical in shape with AuNPs appearing as black dots floating on the surface, and had a uniform particle size distribution, primarily around 100 nm, as observed by TEM (Figure 4B). Further examination with DLS analysis suggested that the particle size ranged primarily from 78 nm to 122 nm with an average value of 91.28±12.1 nm (Figure 4C), and had size distribution polydiversity index smaller than 0.121. The embedment of AuNPs in the liposome membrane under laser excitation significantly enhanced the permeability of the liposome and triggered more efficient 5178 release (74.53%±1.63% in 40 minutes, red solid curve) than liposomes without AuNPs (14.53%±3.17% in 40 minutes, black solid curve) or AuNP-liposomes without excitation (21.92%±2.08% in 40 minutes, red dot curve) in vitro (37°C water bath) as shown in Figure 4D. effect of liposome encapsulation on diffusion of fluorophores in tumor Malignant xenografts (MDA-MB 231 cell/matrigel™) were implanted subcutaneously into male nu/nu nude mice and allowedtogrowintoasolidmasswithdiameterfrom1cmto2cm. After anesthesia, the mice received a 50 μL bolus injection of either 1 mM fluorescein aqueous solution or 1 mM fluorescein encapsulated in AuNP-liposomes (the equivalent fluorescein concentration was 0.25 mM due to the dilution effect after purification with size-exclusive gel filtration to remove unencapsulated fluorescein; the lipid concentration was similarly diluted from 20 mg/mL after hydration to 5 mg/mL after purification). A 1 mM fluorescein aqueous solution was 8 1 0 2 l u J 2 1 n o 7 5 1 . 9 2 1 . 6 9 1 . 5 y b / m o c . s s e r p e v .do l.y //www seon :s lu tp a th on s rom rpe fded roF a o l n w o d e n i c i d e m o n a N f o l a n r u o J l a n o it a n r e t n I chosen because it had the highest concentration-dependent fluorophore (within or without liposome) injection, such as quantum yield, providing the strongest signal in studying the 0.5 at 0+ minute and 30 minutes, 0.25 at 60 minutes, and diffusion of fluorophores (within or without liposome) by 0.071 at 120 minutes for the 1 mM fluorescein group (Figure fluorescent imaging. The time-dependent diffusion patterns 7A) or 0.5 at 0+ minute and 30 minutes, 0.3 at 60 minutes of fluorophores (within or without liposome) were monitored and 120 minutes for the liposome group (Figure 7B). The by in vivo planar fluorescence imaging. The tumor boundary normalized fluorescence at the tumor area was calculated was delineated with specific fluorescence contour levels of by dividing the sum of the fluorescence intensities of the pixels on bright-field (BF) images of mice at times after pixels in the tumor (above the threshold contour level) at Figure 7 (Continued) submit your manuscript | www.dovepress.com Dovepress 5179 fded roF a o l n w o d e n i c i d e m o n a N f o l a n r u o J l a n o it a n r e t n I a specific time by the sum at 0+ minute (Figure 7C). It was found that liposome encapsulation yielded approximately 81% fluorophore retention (estimated by the normalized fluorescence intensity at the 120th minute) in the tumor 120 minutes after fluorophore injection (Figure 7C, red curve), while less than 14% free fluorophore retention was observed in the tumor 120 minutes after fluorophore injection (Figure 7C, green curve). Fiber-optic guided laser excitation triggered liposome release in vivo Fiber-optic guided laser excitation triggered liposome releases in vivo were investigated with the xenograft mice model mentioned above. After anesthesia, the mice received a 50 μl bolus injection of 75 mM fluorescein aqueous solution encapsulated in AuNP-liposomes. A 10-minute duration of CW laser excitation was selected for consecutive tunable 5180 8 1 0 2 l u J 2 1 n o 7 5 1 . 9 2 1 . 6 9 1 . 5 y b / m o c . s s e r p e v .do l.y fded roF a o l n w o d e n i c i d e m o n a N f o l a n r u o J l a n o it a n r e t n I release (with ~50% fluorescein remaining in the liposome significant (+42%, [normalized fluorescence 0+ minute after after the first triggered release, see Figure 4D, red curve). The excitation–normalized fluorescence before excitation]/nortumor boundary was delineated with specific fluorescence malized fluorescence before excitation) normalized fluorescontour levels of pixels on bright field images (BF) of mice cence increase at the tumor area immediately after 10 minutes at times after 75 mM fluorescein in AuNp-liposome injecof excitation (Figure 8B, red curve), while liposome without tion, such as 0.5 before laser excitation, and 1, 0.4, 0.4 at 0+, excitation had gradually declined normalized fluorescence 60, 120 min (Figure 8A). The laser excited liposomes had a at the tumor area (Figure 8B, blue curve). submit your manuscript | www.dovepress.com Dovepress 5181 8 1 0 2 l u J 2 1 n o 7 5 1 . 9 2 1 . 6 9 1 . 5 y b / m o c . s s e r p e v .do l.y //www seon Potential of the delivery system for :s lu th on tunable release tp a s rom rpe Upon consecutive fiber-optic guided laser excitation of 75 mM fded roF liposome-encapsulated fluorescein in vivo, a significant lnoa (72%, [normalized fluorescence at 60th minute – normalized dow fluorescence at 50th minute]/normalized fluorescence at iicened t5u0mthormarineautiem)mfleudoiareteslcyeanfcteeritnhcerfeiarsste1w0amsinoubtseesr(v5e0dtha–t60ththe onm minutes, Figure 9A) of laser excitation, while a relatively faN milder fluorescence increase (33%, [normalized fluorescence loa at 120th minute–normalized fluorescence at 110th minute]/ n ruo normalized fluorescence at 110th minute) was observed after lJna the second 10 minutes (110th–120th minutes, Figure 9A) of itoa laser excitation (Figure 9C), which was consistent with accutrne mulation fluorescein quantity upon consecutive fiber-optic In guided laser excitation of 75 mM liposome-encapsulated fluorescein in vitro (rat plasma) as shown in Figure 9B. Discussion The fiber-optic guided laser excitation triggered content release from AuNP-embedded liposomes was characterized both in vitro and in vivo. The hair-size (200 μm) optical fiber was found to be capable of triggering sufficient release when conveying 65 mW CW diode laser excitation with time intervals of minutes, not only in biomimetic 37°C saline solutions but also in xenograft tumors. This study demonstrated for the first time the triggered release of selective content from AuNP-embedded liposomes in vivo. Because of their proven biocompatibility and efficient photo-thermal conversion through surface plasma 5182 submit your manuscript | www.dovepress.com Dovepress resonance, AuNPs (cluster, nanoshell) have previously been deposited on the liposome membrane outer surface, tethered to the liposome membrane, or entrapped within the liposome cavity for remotely triggered content release through wavelength-specific light excitation from the ultraviolet to near infrared region.39–42 However, no studies have reported their corresponding content release efficiencies triggered by light excitation in vivo. This may be due to challenges caused by the inconsistent results of in vivo non-invasive irradiation from varying subject/disease conditions (such as tumor size and location).30 Our preliminary results proved that the transmission of external energy (laser excitation) through thin fibers (replacing propagation through inhomogeneous tissue) can eliminate the limited penetration efficiency and subject-dependent inconsistency of the conventional noninvasive external trigger systems (which still require invasive chemotherapy administration by intravenous or intratumoral injection) mentioned above,17,18,25–27 while yielding standard errors of excitation triggered release (Figure 8B) in a range (defined by the percentage of the normalized signal) similar to that of diffusion errors (Figure 7C). Both standard errors originated primarily from deviations of diffusion caused by subject-dependent bio-medium conditions, and fiber-optic guided excitation did not contribute further fluctuations to triggered releasing profiles. The illumination covered the whole area of tumors with diameters up to 2 cm (Figure 1B). The tunable delivery was controlled by the duration of excitation (light exposure time) as shown in Figure 4D, but could be further regulated by modulating laser output power/amplitude (total light dosage) or excitation pattern (light delivery mode). 8 1 0 2 l u J 2 1 n o 7 5 1 . 9 2 1 . 6 9 1 . 5 y b / m o c . s s e r p e v .do l.y This could be used to overcome deviations owing to subject/disease conditions (such tumor size and location); further bedside dosage fine-tuning during procedure could be provided by pairing with minimally invasive fiber-optic monitoring of drug-induced apoptosis activity function as mentioned above.22–24 The tunable delivery through liposome was also found superior than the conventional dropwise intravenous or intratumoral injection because of dosage retention and side effect reduction. From the in vivo fluorophore diffusion studies (Figure 7), encapsulation in liposomes enabled the retention of more than 80% of the injected fluorescein (5.79 times higher than fluorescein administered without liposomes) after 120 minutes. For the group with fluorescein administered without liposomes (Figure 7A), a significant amount of the simulated drug-biodistribution marker escaped from the tumor through leaky neovascular tumor-to-circulation transfer, unlike the payload encapsulated in liposomes, which had a bulkier volume and lower mobility (or a reduced transfer efficiency through neovascular pores). Up to a 10% normalized dosage (compared with the highest concentration accumulated in the tumor at 0+ minute) was readily spread systematically through the circulation between 30 and 60 minutes after injection (Figure 7A), but not in the liposome group (Figure 7B). This result indicated that the intended burst discharge profiles being developed for most internal and external trigger systems could result in undesired lateral damage on exposed non-target tissue. The active release mechanism should be fine-tuned by the minimally invasive fiber-optic monitoring described above to steadily maintain the released therapeutic dosage (subject/patient dependent) for an extended period. In addition, the experimental tunable chemotherapy agent delivery platform delivers photo-thermally responsive liposomes directly into the tumor for more efficient tumor-specific accumulationand replaces conventional systematic intravenous administration, which is unreliably effective because of the subject-dependent differences in systematic elimination and lesion tissue absorption of therapeutic agents.4 This design could also circumvent the limited penetration of anticancer agents into tumor tissue by conventional intravenous administration (with or without delivery vesicles) due to the high interstitial pressure of cancerous tissues.16,19 These therapeutic improvements will be verified by future in vivo studies delivering chemotherapy agents in place of the fluorescein used in this research with optical imaging, such as photo-acoustic imaging, interrogating the time-dependent biodistribution of AuNP-liposomes, treatment-related morphological or hemodynamic changes of tumor, or tumor suppression indices (volume and metastasis reduction) of luminescent cancer cell line xenografts. We anticipate future cancer theragnosis, such as a laparoscopic treatment for pre-operation of tumors before their surgical removal, combining the personalized chemotherapy system (in which tunable drug delivery is adjusted by real-time minimally invasive drug-induced biomarker monitoring) to optimize therapeutic efficacy. The fiber-optic cable of laparoscopy for viewing of the affected area from distant can be applied to convey the laser excitation for triggered release of the AuNP-liposome and returning fluorescence signal for assessing drug-induced apoptotic activity. Conclusion We report in vitro and in vivo characterizations of a proposed tunable chemotherapy system with hair-size microcapillaries delivering photo-thermally responsive liposomes directly into tumors and fiber-optic guided laser excitation to trigger the tunable release of these liposomes. The content release profile was quantified by the increase of fluorescence resulting from the dilution of the released self-quenching fluorescein encapsulated in liposomes. In in vitro studies indicated that AuNP-embedded liposomes triggered more efficient triggered release than the traditional temperature-responsive liposome. Using in vivo mouse xenograft studies demonstrated that the encapsulation of fluorescein in liposomes resulted in a more substantial compound retention in the tumor and suggested the tunable release capability of the system by triggering consecutive releases with fiber-optic guided laser excitations. Acknowledgments The authors wish to thank Chief Dr Chun-Ru Dai (R&D Department, China Medical University, Taichung, Taiwan) for his kindly assistance with in vivo fluorescence imaging acquisition. The research was funded by National Science Council of Taiwan (NSC 97-2218-E-005-096). Disclosure The authors report no conflicts of interest in this work. submit your manuscript | www.dovepress.com Dovepress 5183 8 1 0 2 l u J 2 1 n o 7 5 1 . 9 2 1 . 6 9 1 . 5 y b / m o c . s s e r p e v .do l.y fded roF PowerdbyTCPDF(w w.tcpdf.org) submit your manuscript | www.dovepress.com Dovepress //www seon Publish your work in this journal The International Journal of Nanomedicine is an international, peerreviewed journal focusing on the application of nanotechnology in diagnostics, therapeutics, and drug delivery systems throughout the biomedical field. This journal is indexed on PubMed Central, MedLine, CAS, SciSearch®, Current Contents®/Clinical Medicine, Journal Citation Reports/Science Edition, EMBase, Scopus and the Elsevier Bibliographic databases. The manuscript management system is completely online and includes a very quick and fair peer-review system, which is all easy to use. 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Huei-Ling Huang, Pei-Hsuan Lu, Hung-Chih Yang, Gi-Da Lee, Han-Ru Li, Kuo-Chih Liao. Fiber-optic triggered release of liposome in vivo: implication of personalized chemotherapy, International Journal of Nanomedicine, 2015, 5171-5185, DOI: 10.2147/IJN.S85915