Sustained intrathecal delivery of amphotericin B using an injectable and biodegradable thermogel

Abstract Cryptococcal meningitis is a fungal infectious disease with a poor prognosis and high mortality. Amphotericin B (AMB) is the first choice for the treatment of cryptococcal meninges. The blood-brain barrier (BBB) is the major barrier for the effective delivery of drugs to the brain. In this study, AMB was incorporated in a thermosensitive gel for intrathecal injection. We first synthesized AMB-loaded thermogel, investigated its in vitro cumulative release, and in vivo neurotoxicity, and therapeutic effect. The thermosensitive gel was comprised of 25 wt% poly (lactic acid-co-glycolic acid)-poly (ethylene glycol)-poly (lactic acid-co-glycolic acid) (PLGA-PEG-PLGA) triblock polymer aqueous solution. The AMB loaded in the thermosensitive gel (AMB in gel) had low viscosity at low temperature and resulted in the formation of a non-flowing gel at 37 °C (physiological temperature). AMB loading in gel sustained its release for 36 days and the in vitro cumulative release rate was satisfactory. Compared with the AMB solution, intrathecal administration of AMB in gel could reduce the neurovirulence of AMB and get a better treatment effect. The findings of the current study show that the injectable PLGA–PEG–PLGA thermogel is a biocompatible carrier for the delivery of drugs into the intrathecal.


Introduction
Cryptococcal meningitis (CM), an opportunistic fungal infection caused by Cryptococcus neoformans or Cryptococcus gattii, is a fatal central nervous system (CNS) disease with a worldwide distribution. CM is the leading adult meningitis in areas with a high incidence of HIV (Rajasingham et al., 2017;Williamson et al., 2017). Besides, it also shows a growing number of immunocompromised and immunocompetent patients. In the USA, the death rate in HIV-negative CM individuals was around one quarter of CM-associated hospitalizations and one-third of CM-associated mortalities (Perfect et al., 2010;Williamson et al., 2017;Migone et al., 2018).
AMB, a member of polyenes, is the first-recommended drug for the treatment of CM (Williamson et al., 2017). The pharmacokinetics studies have shown its poor penetration into the cerebrospinal fluid (CSF) and brain parenchyma due to its molecule properties (Hamill, 2013) and blood-brain barrier (BBB). BBB is an impermeable cellular interface that separates the blood from the brain, selectively allows only a few substances to pass. The concentration of AMB in CSF was approximately 0.05 mg/L following its intravenous injection, 10 times lower than used for antifungal activity (Nau et al., 2020). Besides, its intravenous administration has many side effects such as headache, fever, damage of liver and kidney, and vasculitis, etc (Nau et al., 2020)., which makes it far from being the best choice.
New therapeutic approaches including intrathecal injection increase the concentration of AMB in CSF. However, they are required to be performed by lumbar puncture 2-3 times a week with inevitable neurological toxicity symptoms like headache, neck stiffness, lower limb pain, urinary retention, and even lower-limb paralysis. Intraventricular infusion with Ommaya reservoirs (Nakama et al., 2015) and lumbar puncture drainage (Yuchong et al., 2011;Fang et al., 2012) of AMB has been reported to control CM effectively, a 1-h intrathecal infusion rather than injection could reduce neurotoxicity, however, it is easy to cause superinfection and more nursing care is needed. The ideal therapeutic drugs are supposed to have a high concentration in the brain tissue or CSF and fewer side effects.
Hydrogels have been a hot spot in the research of DDS. Various studies have been recently reported about hydrogels injected into the intrathecal space or rat spinal cords (Ho et al., 2019;Householder et al., 2019;Song et al., 2019). It has been demonstrated that biodegradable PLGA pellets can effectively release drug and do not require surgical removal post drug release (Wilems & Sakiyama-Elbert, 2015). Yuanfei Wang et al. (2013), encapsulated PEGylated epidermal growth factor (PEG-EGF) in PLGA nanoparticles and erythropoietin (EPO) in PLGA-poly (sebacic acid) core-shell biphasic microparticles. The dispersion of EGF-PEG and EPO polymeric particles in a hyaluronan/methyl cellulose (HAMC) hydrogel that sustained the release of EPO for one week and EGF for three weeks continuously and inhibited the inflammatory reactions of brain tissues (Wang et al., 2013). Nano-polymer materials are expected to replace traditional drug delivery systems as a more promising approach to continuous intrathecal administration.
For the above, we propose that PLGA-PEG-PLGA triblock copolymers can be used to load AMB and inject into subarachnoid space by lumbar puncture. In this way, PLGA-PEG-PLGA triblock copolymers served as a DDS for the continuous release of AMB in CSF. In this research, we first synthesized PLGA-PEG-PLGA triblock polymers and determined their properties. The synthesized triblock polymers were then used for obtaining AMB-loaded thermogel. Further, we assessed the rheology, in vitro cumulative release, and its neurotoxicity, and the therapeutic effect in a rat model of CM.

Materials and animals
Polyethylene glycol (PEG, MW: 1500), stannous octoate (Sn(Oct) 2 , 95%), AMB, and AMB soluble were procured from Sigma-Aldrich. D, L-Lactide (LA), and glycolide (GA) were bought from Purac. Purified deionized water was obtained via Milli-Q plus system from Millipore (Bedford, USA). C. neoformans reference strain H99 (serotype A) was kindly donated by Dr.John Perfect lab. Latex-crytococcus antigen detection system was provided by IMMY (USA). Acetonitrile (ACN) was of HPLC grade, while all other chemicals were of analytical grade.
Male Sprague Dawley rats having 250-300 g bodyweight were provided by the Naval Medical University Laboratory Animal Center (Shanghai, China) and were nourished in our specific pathogen-free (SPF) animal facility. The in vivo experimental procedures were performed according to the national guidelines and the approval was provided by the Animal Care and Use Committee at Institute Pasteur of Shanghai.

Synthesis and characterization of PLGA-PEG-PLGA copolymer
PLGA-PEG-PLGA triblock copolymer was synthesized via ringopening polymerization of GA and LA with PEG as the macroinitiator and Sn(Oct) 2 as the catalyst (Yu et al., 2009. PEG 1500 (20.0 g) was placed in a three-necked flask and the remaining water of polymer was removed at 130 C under vacuum for 3 h followed by cooling to 100 C by passing argon. Then, LA (35.3 g) and GA (11.3 g) were added and the mixture was stirred well. A toluene solution containing 60 mg of Sn(Oct) 2 was then added to the mixture. The removal of toluene was carried out under vacuum for 15 min, and the reaction was carried out at 150 C for 12 h in the presence of argon. When the reaction was complete, the flask was kept at 110 C for the removal of unreacted monomers (for 3 h). In the end, the resultant copolymer was washed thrice with deionized water at 80 C followed by freeze-drying for the removal of residual water.

1 h-NMR measurement
Structural elucidation and composition of the synthesized polymer were carried out with 1 H-NMR (Bruker BioSpin International, AVANCE III HD 400 MHz) (Yu et al., 2011). Tetramethylsilane (TMS) and CDCl3 were used as the internal standard and the solvent, respectively.

Gel permeation chromatography characterization
A gel permeation chromatography (GPC) system (Agilent 1100) was employed to identify the MWs and the distributions of the PLGA-PEG-PLGA triblock copolymers (Yu et al., 2011). The measurements were conducted at 35 C, using tetrahydrofuran as a solvent with a flow rate of 1.0 mL/min. Monodispersed polystyrene was utilized as a standard for the calculation of MWs.

Determination of sol-gel transition temperature
The sol-gel transition temperature of the polymer aqueous solutions was measured by an inverted rotation method (Li et al., 2013). A series of polymer solutions of different concentrations were prepared. The polymeric solution (0.5 mL) was transferred into a test tube (2 mL), followed by immersing in a water bath at 24 C. When the temperature was elevated by 1 C, the test tubes were inverted by 180 to examine the flow of liquid. When the visible flow was not observed within 30 s, the sample was regarded as a gel state. The above-inverted rotation method was repeated until the sol-gel phase transition occurred in all concentrations of the sample.

Rheological analysis
The rheological behavior of copolymer aqueous solution (25 wt%) and AMB-loaded copolymer aqueous solution (2, 4, and 8 mg/mL) with temperature was measured by rotational rheometer (Malvern, Kinexus Pro). The lamina acted as a clamp for samples (cone angle was 1 degree, the diameter was 60 mm) while keeping the clearance as 0.03 mm, angular velocity as 10 rad/s, the rate of heating as 0.5-degree C/min, and the temperature range as 15-50 C (Yu et al., 2009). To prevent moisture volatilization during heating, silicone oil was evenly applied to the periphery of the fixture.

In vitro release of drug
Ultraviolet spectrophotometry was used to measure the cumulative release rate of AMB in gel with different concentrations in vitro. AMB-loaded copolymer aqueous solutions (2, 4, and 8 mg/mL, 0.5 mL of each one) were placed at the bottom of the glass tube, and 3 groups of parallel samples were set for each concentration. The temperature of the water bath was maintained at 37 C. Post transformation of AMBloaded polymer solution into the hydrogel, 10 mL of PBS having SDS (1%) and tween (0.5%) were added into a glass tube as the releasing medium (pH 7.4). All sample tubes (9 groups in total) were taken out of slow-release media (10 mL) at a specific time point and added 10 mL of fresh PBS solution at the same temperature. The drug residue in the release media was determined by an ultraviolet spectrophotometer. The release data was evaluated by the first-order release curve, whose equation is ln(1-M t /M 1 ) ¼ -Kt (Xiao et al., 2014;Yang et al., 2014;Xie et al., 2015). Here, M t is the cumulative release at time t and M 1 is the cumulative release at time infinity. The release rate constant k is associated with the diffusion coefficient, chemical structure of hydrogel, and some geometric parameters.

Toxicology evaluation
The rats were intrathecally injected with AMB in the gel to assess their toxicology through Tarlov's scores (Tarlov, 1972) and survival rate in rats. All rats were randomized into four groups (eighteen rats in both the thermogel group and solution group and eight rats in the blank gel and NS group). The rats were anesthetized with pentobarbital (40 mg/kg) by intraperitoneal injection. For AMB in the gel group, an aliquot of 100 uL AMB-loaded thermogel (8 mg/mL) was injected into the subarachnoid space. The syringe was held for about 30 s to allow the solution to form a semi-solid gel and make sure no CSF bleeding occurred during the procedure. For the AMB solution group, 100 ul of 8 mg/mL AMB solution was injected into the subarachnoid space and the syringe held for about 30 s. The same volume of blank gel and NS was injected into the subarachnoid space for the blank gel and NS group, respectively. All the formulations were sterilized by filtration before administration. The vital signs were observed and every limb's motor activity was evaluated after administration by the modified Tarlov's scores (Tarlov, 1972;Shi et al., 2007): 0, complete paralysis or death; 1, muscle tension, free movement, not weight-bearing; 2, affected limbs can be weight-bearing and standing; 3, can stand normally, may limp, when walking, the limb has tow; 4, normal muscle strength. The scores of each limb were added and the total scores were recorded. On the 7th day after administration, all the rats were sacrificed and the spinal cord near the injection site was cut. The variations in spinal cord nerves were observed via Hematoxy-Eosin (HE) staining.

Treatment effect
The therapeutic effects were evaluated by detecting the number of cryptococcus and latex agglutination test (LAT) in CSF. A rat model of cryptococcal meningitis was established (Najvar et al., 1999;Fries et al., 2005;Carroll et al., 2007). C. neoformans reference strain H99 (serotype A) was recovered from À80 C. A concentration of 2 Â 10 8 CFU/mL bacteria suspension was prepared, and 50 uL of the bacteria suspension was injected into intracranial to build cryptococcal meningitis rat model. The same volume of CSF was taken before injection for maintaining intracranial pressure (Fries et al., 2005). All rats were grouped into four randomized sets (six rats in each group). One group was a sham operation group. A cryptococcal meningitis rat model was established for the other three groups. On the 7th day after inoculation, 100 uL of AMB-load thermogel (8 mg/mL) was injected into the subarachnoid space for AMB in the gel group and 100 uL of blank thermogel were injected into the subarachnoid for the blank gel group. For the AMB solution group, 100 uL of 0.01 mg per mL, 0.02 mg per mL, 0.03 mg per mL, and 0.04 mg per mL AMB solutions were injected intrathecally at 7, 11, 15, and 19 days after infection to simulate the clinical treatment regimen. On 14 and 21 days, 100 ul CSF was taken for CSF culture and a LAT was carried out to compare treatment effects.

Statistical analysis
The obtained results were represented as mean ± SD. The survival rate was measured by the Log-rank test. T-test was used for samples conforming to the normal distribution. A non-parametric test was employed for samples not conforming to the normal distribution, and p-value < .05 revealed a statistical difference.

Synthesis and characterization of PLGA-PEG-PLGA triblock copolymer
PLGA-PEG-PLGA triblock copolymer was synthesized by ringopening copolymerization of LA and GA using PEG as the macroinitiator in the presence of Sn(Oct) 2 . The chemical structure of the triblock polymer is shown in Figure 1(A). 1 H NMR spectrum of the polymer is depicted in Figure 1(B). In the LA unit, the characteristic peaks of the methyl and methine protons were at 1.55 and 5.20 ppm, accordingly while in the GA and PEG units, the characteristic peaks of methylene protons were at 4.80 and 3.60 ppm, accordingly. At 4.31 ppm, the peak of the methylene protons of the PEG segment (nearby PLGA blocks) was found. The integral peaks at 5.20, 4.80, and 3.60 ppm indicated the number-average MW (M n ), LA/GA molar ratio, and PEG/PLGA molar ratio, respectively which had been described in the previous studies (Yu et al., 2007(Yu et al., , 2009(Yu et al., , 2011. The MW of the copolymers was approximately 5000. As shown in Figure 1(C), the GPC trace revealed a unimodal distribution and the dispersity was 1.28, indicating the polymerization was under control and the ideal polymer was synthesized. Molecular parameters of the copolymer determined by 1 H NMR and GPC are indicated in Table 1.

Sol-gel transition of the aqueous solutions of the PLGA-PEG-PLGA triblock copolymer
The phase diagram of the systems is shown in Figure 2(A). The systems went through three stages with the increasing temperature: first formed free-flowing sols state, then transformed to a semi-solid gel state, and finally went to suspension. The critical gelation concentration (CGC) of the systems was about 12 wt%. The phase transition temperature of 25 wt% polymer aqueous solution was around 33.5 C. It means that when the temperature is below 33.5 C, the 25 wt% polymer aqueous solution is in a solution state and can be used for injection and drug loading. When the temperature is above 33.5 C and is lower than 40.5 C, it is in a gel state and can be used for sustained-release of drugs. The human body's temperature is about 37 C. Therefore, we selected 25 wt% polymer aqueous solution as the drug loading system. As shown in Figure 2(B), the polymer aqueous solution has a low modulus at low temperature, indicating that the system has good injectability. As the temperature increases, the storage modulus G 0 and the loss modulus G 00 rise sharply near the phase transition temperature, indicating that the system forms a gel. According to the intersection of energy storage modulus and loss modulus as the definition of the sol-gel transition temperature, it can be determined that the gel-forming temperature is about 34 C (Luan et al., 2018), which is close to the result of the phase diagram. As shown in Figure 2(C), the storage modulus G 0 and the loss modulus G 00 did not change significantly in blank gel and AMB in gel, and the sol-gel transition temperature is still the same. This means that the AMB did not affect the thermogel. Figure  2(D) shows the visual changes of the blank gel and AMB in the gel as the temperature rises to 37 C.   the sudden release of AMB in the gel at 2 mg per mL, 4 mg per mL, and 8 mg per mL was 1.6%, 1.3%, and 1.5%, respectively, while the cumulative release at 36 days was 89.0%, 77.1%, and 65.6%, respectively. It can be suggested that the loading concentration has little effect on the sudden release of drugs. But with elevation in the loading concentration, the cumulative release was lowered. The AMB in gel continued to release the drug slowly for 36 days. The first-order fitting results of AMB slow-release data are shown in Table 2. The three curves are consistent with the equation, and the correlation coefficient R 2 has been greater than 0.95. This property indicates that the diffusion of the drug and the degradation of the gel are the main reasons for the slow release.

Toxicology evaluation
The Tarlov's scores of the four groups of rats are shown in Table 3. All the rats had normal limb movements before administration. The Tarlov's scores of the limbs of rats in the blank gel group and the NS group were 16 ± 0 points each day. The daily Tarlov's scores of the limbs of rats in AMB in the gel group were found to be elevated than those in the AMB solution group (p < .05), revealing that the toxicity of AMB in the gel to the spinal cord was less than that of the AMB solution.
The survival rate of the rats was shown in Figure 4(A). There was no death in the blank gel group and the NS group, and the 7-day survival rate was 100%. In the AMB in the gel group, 1 rat died on the 5th day after administration, and the 7-day survival rate was 94.4%. Eight rats in the AMB solution group died on the day of administration, followed by death every 1-2 days, with a 7-day survival rate of 27.8%.
The survival rate of the AMB in the gel group was significantly elevated relative to the AMB solution group (p < .05), indicating that thermogel could reduce the mortality caused by neurotoxicity.
The H&E staining of the spinal cord exposed to different groups is shown in Figure 4(B). AMB solution group showed that the injury site was mainly in the posterior cord of white matter. The boundary between gray and white matter was found to be not clear, some nerve fibers dissolved and disappeared, and the loose tissues underwent edema, while some cells showed vacuolar degeneration and karyopyknosis. The AMB in the gel group exhibited a clear boundary between gray and white matter, a small amount of fiber disorder, and cellular vacuolar degeneration. NS and blank gel group exhibited the regular morphology. Figure 5(A) depicts the results of CSF culture on the 14th and 21st days after rat modeling, respectively. On day 14, the bacterial loads of the blank gel group, the AMB solution group, and the AMB in the gel group were found to be 49,500 ± 23,855 CFU/mL, 39,667 ± 12,140 CFU/mL, and 17,000 ± 48,757 CFU/mL, respectively. On day 21, the bacterial loads of the blank gel group, the AMB solution group, and the AMB in the gel group were found to be 72,600 ± 15,059 CFU/mL, 41,333 ± 20,490 CFU/mL, and 3000 ± 1786 CFU/mL, respectively.

Treatment effect
The LAT is a sensitive indicator to detect the antigenic titer of the cryptococcus polysaccharide capsule. As evident from Figure 5(B), from day 14 to day 21, the average titer of the blank gel increased from 1:453 to 1:844 (p < .05), the average titer of the AMB solution increased from 1:22.6 to 1:32 (p > .05), and the average titer of the AMB in gel decreased from 1:89 to 1:28 (p < .05). It can be seen from the figures that the results of LAT were consistent with the results of CSF culture in both longitudinal and lateral comparisons, which verified that the therapeutic effect of AMB in the gel was superior to that of AMB solution again.

Discussion
AMB is an irreplaceable drug for the treatment of CM, however, patients mostly discontinue the medication because they are unable to tolerate its side effects. There are many studies aimed at improving AMB efficacy and reducing its toxicity (Zumbuehl et al., 2007;Hudson et al., 2010;Asthana et al., 2015;Kumar et al., 2015;Sosa et al., 2017), however,  they have not been advantageous over the thermosensitive PLGA-PEG-PLGA hydrogel. Firstly, the structure and properties of thermosensitive PLGA-PEG-PLGA hydrogel are more suitable for loading hydrophobic drugs. AMB is extremely difficult to dissolve in water and can be well wrapped in a hydrophobic region with nearly 100% entrapment efficiency. Secondly, the PLGA-PEG-PLGA hydrogel has good biocompatibility. Its degradation products have already been present in the body and can be completely decomposed and consumed. Thirdly, temperature-sensitive properties allow PLGA-PEG-PLGA hydrogel to be used for injection, and the ideal concentration of AMB can be continuously provided in areas where the fungal infection is serious. Fourthly, the controlled-release characteristics can reduce the dosing frequency. Continuous and ideal drug concentration can kill Cryptococcus, thus leading to effective treatment of the disease. Finally, neurotoxicity associated with AMB high concentration causes irreversible damage to spinal nerves. Intrathecal injection of AMB-loaded thermogel can avoid high AMB concentration and reduce neurotoxicity. All the above properties make AMB-loaded thermogel suitable for intrathecal injection of CM.
PLGA-PEG-PLGA triblock copolymers have been extensively studied for the delivery of drugs. Liraglutide, granulocyte colony-stimulating factor, porcine growth hormone, recombinant hepatitis B surface antigen, and antitumor drugs have been loaded in the thermogel (Matthes et al., 2007;DuVall et al., 2009;Elstad & Fowers, 2009;Tyler et al., 2010;Cho et al., 2016). In our study, a thermoreversible hydrogel comprising of copolymers with different features was prepared as an injectable implant for intrathecal DDS. The PLGA-PEG-PLGA triblock copolymer was synthesized and underwent a reversible sol-gel transition as the temperature elevated. The results showed that the synthesis, structural control, and molecular weight were within expectations (Yu et al., 2009(Yu et al., , 2011. For the preparation of injectable AMB-loaded thermogel, AMB was loaded into the aqueous polymer solution at 4 C, followed by stirring to obtain a homogeneous system. From the microscopic point of view, PLGA-PEG-PLGA is a triblock polymer. The PLGA at both ends of the polymer is hydrophobic and the PEG in the middle is a hydrophilic region, which makes the polymer spontaneously assembled into spherical particles upon contact with an aqueous environment (Yu et al., 2007(Yu et al., , 2009. AMB is a hydrophobic drug and can be entrapped into the hydrophobic region of the thermogel. When the temperature rises to sol-gel transition temperature (33.5 C), the particles interact with each other, thus form a network and become a gel state. This in turn provides increased loading of the AMB in the thermogel.
The result of in vitro release showed that a small part of AMB failed in the process. The higher loading concentration resulted in a higher rate of failure. The factors affecting AMB failure are not only its instability and loading concentration but also temperature and light. However, the AMB solubility has been very low in the water, little AMB is still dissolved in water. The main reason for the sudden release of AMB in the gel is the release of AMB which is dissolved in water. When the thermogel slowly degrades in an aqueous solution, the AMB wrapped in the hydrophobic region is exposed. The AMB concentration in the hydrophobic region is high, while it is very low in the solution. So, AMB will diffuse from high concentration to low concentration, thus it is slowly released (Yu et al., 2008). The gel can release its loaded AMB for 36 days in vitro. PLGA-PEG-PLGA triblock copolymer degrades into ethanol, lactic acid, and glycolic acid, thus it has good biocompatibility.
In the toxicity study of the Tarlov's score, all surviving rats had normal upper limbs. Most of the dead rats had respiratory arrest within 2-3 minutes after administration, followed by cyanosis, and eventually suffocated. The probable reason was that AMB solution diffused from the level of the lower lumbar spine to the thoracic vertebrae and cervical spine, damaged respiratory motor neurons, caused apnea and ultimately lead to suffocation. However, when the AMBloaded thermogel was injected, it turned into a gel state and remained in situ. So, AMB could not diffuse nonspecifically. According to the in vitro release curve, the burst release of 8 mg/mL AMB gel on the first day was 12 ug, much less than that of AMB solution of 800 ug. It can be seen from the above discussion that sustained release and in situ immobilization were the main reasons for reduced neurotoxicity and the high survival rate of AMB in the gel. The result of H&E staining also showed that the AMB in gel could reduce the neurotoxicity of AMB and blank gel resulted in no damage to the spinal cord.
In the pre-experiment, 100 uL of the AMB solution with a concentration of 2 mg per mL was used for intrathecal administration twice a week, four times in total. Most of the rats died on the day after the first administration, and all of the rats died after the second administration. Therefore, it was hard to set up the AMB solution group (2 mg per mL, 100 uL, 4 times) with the same dosage as the AMB-loaded thermogel (8 mg per mL, 100 uL, once) for pharmacodynamic comparison. Clinically, the AMB solution is injected intrathecally 2-3 times a week according to the patient's condition, starting from 1 mg and increasing by 1 mg each time until the patient is intolerant and maintaining this dose. In this study, according to the clinical administration mode and the volume ratio of CSF between humans and rats, we added the corresponding dose of soluble AMB to the CSF of rats to simulate the clinical treatment as the control group. It can be seen from the results that the AMB solution could keep the number of cryptococcus from increasing, while AMB in the gel can significantly reduce the number and titer of cryptococcus.
Our study has several limitations. Firstly, although rats showed a higher survival rate in AMB in the gel group, one rat died on the 5th day after administration. Therefore, the substantial toxicity of PLGA-PEG-PLGA triblock copolymers could not be ruled out. Secondly, toxicity was evaluated by the modified Tarlov's scores which were mainly based on observation. Thus, the results of the toxicity experiment can be biased. Thirdly, the cumulative release of the drug in vivo may be different from that in vitro, therefore further in vivo investigation is required on pharmacokinetics and therapeutic effect.
Taken together, as compared to the traditional treatment regimen, AMB-loaded thermal was found to be convenient, and more effective with less neurotoxicity. The PLGA-PEG-PLGA triblock copolymers are biocompatible and can effectively deliver an intrathecal drug. Currently, intrathecal hydrogels are widely reported in the repair of spinal cord injury. Dongfei Liu et al. (2016), reported an in-situ gelling drug delivery system, comprising a Poloxamer-407, a 188 mixturebased thermoresponsive hydrogel matrix and, an incorporated bioactive compound (monosialoganglioside, GM1), for spinal cord injury therapy. The thermoresponsive hydrogel delayed the GM1 release for around one month. Irja Elliott Donaghue et al. (2015), reported HAMC hydrogel, an injectable and biodegradable polymeric nanoparticle, as an injection into the intrathecal space for acute local delivery. Neurotrophin-3 was encapsulated in the hydrogel and its in vivo release was observed for 28 d.
AMB plays an important role in the treatment of CM. It is of great significance to increase the concentration of AMB in CSF for CM. Intrathecal injection of AMB-loaded hydrogel can not only enhance the concentration of AMB in CSF but also greatly reduce the neurotoxicity of AMB. Its sustained-release can minimize dosing frequency and improve patient compliance, thus suggesting the hydrogel as an ideal drug delivery system for the treatment of CM. CM is hard to be treated effectively due to its high recurrence rate and unsatisfactory therapeutic efficacy. The AMB-loaded hydrogel is a breakthrough in the treatment of CM. In this study, CM was used as a model to explore the new route of intrathecal administration.

Conclusion
In the present study, an intrathecal DDS was developed for the treatment of CM. Thermosensitive injectable PLGA-PEG-PLGA hydrogel was fabricated based on a practical blending approach and was then employed to deliver AMB. The AMBloaded thermogel could release AMB for 36 days in vitro with a high cumulative release rate. The in vivo studies showed that intrathecal injection of AMB in gel could reduce its dosing frequency and associated neurotoxicity, and improve the antifungal efficiency. Intrathecal administration of AMB in the gel is a very effective antifungal therapy for the CNS, which provides a good reference for intrathecal drug delivery.