LAL test and RPT for endotoxin detection of CPT-11/DSPE-mPEG2000 nanoformulation: What if traditional methods are not applicable?

Endotoxin detection is an important step in drug characterization. Herein we found that a chemotherapeutic drug nanoformulation composed of irinotecan hydrochloride (CPT-11) and an amphiphilic molecule DSPE-mPEG2000 can interfere with the limulus amebocyte lysate assay (LAL). Furthermore, the rabbit pyrogen test (RPT) results indicated that at a relatively high dosage, the drug irinotecan hydrochloride can induce a hypothermia effect which may render the RPT results ambiguous in determination of the safety of the drug formulation.Our findings demonstrate limitations of endotoxin detection in micellar drugs, and call for the necessity of developing reliable endotoxin detection methods that can overcome the interference of nanomaterials in order to better ensure the drug safety of patients in future pharmaceutical drug development.

Introduction

Endotoxin refers to contaminants such as lipopolysaccharide (LPS) found in the gram-negative bacterial cell wall [1], [2]. As a powerful immunostimulant, endotoxin can activate a variety of mammalian immune cells once in the body especially the circulatory system and trigger excessive secretion of a wide range of cytokines. This can cause multiple organ failure or septic shock and even mortality for patients. Endotoxin contamination is a significant problem all over the world which affects hundreds of thousands of patients every year [3]. In addition, endotoxin is extremely stable and can endure extreme pH, high temperature and even autoclaving. Accurate detection and strict control of endotoxin is therefore a critical step in both fabrication and quality control of medical products [4].

Endotoxin can be measured mainly by two methods: the rabbit pyrogen test (RPT) and limulus amebocyte lysate (LAL) assay [5], [6]. The RPT was first developed and is an in vivo assay based on the fact that endotoxin induces elevated body temperature in rabbits and the detection limit can be as low as 0.5 EU/ml (1 EU = 1 Endotoxin Unit). Although requirement for animals, the experiment design and the judgment for positive results are slightly different from country to country, the goal of the test is the same. Today RPT is still required for some medical products in China and other countries. LAL test was discovered in 1970s and has now been adopted by most countries for detection of endotoxin [7]. It is an in vitro test based on the fact that protein extracts from horseshoe crab (Limulus polyphemus) amebocytes can clot in contact with endotoxin. Since its discovery, the LAL test has grown rapidly and has now replaced RPT as the main method for endotoxin detection for parental products in China. The LAL test is carried out in three different formats including the gel-clot assay, chromogenic test and turbidity test, and the gel-clot assay is the most common method.

In recent years, nanotechnology has been widely pursued as a new route to formulate small molecule chemotherapeutic drugs to lower the systematic toxicity, improve the pharmacokinetic profiles and enhance the therapeutic efficacy especially in cancer treatment [8], [9], [10]. With more and more nanomaterials applied to medical products, it has become increasingly necessary to consider the influence of nanomaterials on detection of endotoxin [11], [12]. Multiple physical and chemical properties of nanomaterials such as the composition, size, shape, surface charge and targeting ligand, etc. can play a role in interacting with LPS and interfering with the test, generating false positive or negative results [13], [14], [15], [16], [17]. Given the application of nanomaterials in nanomedicine, nanosafety assessment, in particular, the safety problems of nanodrugs before clinical application, is becoming increasingly important. At present, most of the detections of endotoxin are focused on empty nanocarriers or pure drugs, and there is limited endotoxin detections of drug-load nanoparticles. In addition, some researchers suggested that pyrogen test could be used when LAL detection was not applicable [18]. However, due to the complexity of the nanoformulation, if there is interference in the detection of LAL test, pyrogen test may not be able to reflect the real results. Herein we demonstrate the issues with endotoxin detection of an irinotecan hydrochloride (nano) micelle (CPT-11/DSPE-mPEG2000 micelle) formulation which was developed by our group for the treatment of advanced colorectal cancer. Our research has guiding significance for the clinical application of nanomedicines and also provides a reference for the study of micellar drugs of class PEG. Results indicated that for the CPT-11/DSPE-mPEG2000 (nano) micelle, both LAL and RPT have their limitations and it is necessary for new methods to be developed to overcome these issues so that accurate evaluation of endotoxin content can be achieved.

Materials and methods

Materials and animals

Samples and reagents: irinotecan hydrochloride (nano) micelles, 40 mg of C33H38N4O6 • HCl (CPT-11), Lot numbers: 20150325DM, 20150427DM, 20150624DM. Limulus reagents are manufactured by three manufacturers: Fuzhou New North Biochemical Industry Co., Ltd. (Specifications: 0.1 ml, Batch number: 13121112, Sensitivity: 0.25 EU/ml); Zhanjiang A&C Biological Co., Ltd. (Specifications: 0.1 ml, Batch number: 1402261, Sensitivity: 0.25 EU/ml and 0.1 ml, Batch number: 1506152, Sensitivity: 0.06 EU/ml); and Xiamen Limulus Reagent Experimental Factory Co., Ltd. (Specifications: 0.1 ml, Batch number: 150208, Sensitivity: 0.06 EU/ml). Bacterial endotoxin working standards are manufactured by National Institutes for Food and Drug Control (Specifications: 80 EU/each, Batch number: 150601–201580). Bacteria and endotoxin free water are manufactured by Zhanjiang A&C Biological Co., Ltd. (Specifications: 30 ml/bottle, Batch number: 1501280) and Zhanjiang Bokang Marine Biological Co., Ltd. (Specifications: 50 ml/bottle, Batch number: 1411150). Animals used in this experiment are Japanese white rabbits (body weight 2-3 kg).

LAL assay

Preparation of samples

According to the clinical instructions, irinotecan hydrochloride (nano) micelle is given intravenously to the patient and can be used either individually or combined with other drugs.

Combination therapy: irinotecan hydrochloride (nano) micelle is administered to patients at 180 mg/m2 through intravenous infusion during 30 to 90 min the first day; leucovorin 400 mg/m2 should be given immediately after the irinotecan hydrochloride (nano) micellar infusion within the same period. After that, 5-fluorouracil can be given through intravenous injection. According to the chinese pharmacopoeia 2015 edition (1143 instruction for bacterial endotoxin test), bacterial endotoxin limit can be calculated as follows: L = K/M, where K is the maximum dose of endotoxin per kg of body weight per h, for injections K = 5 EU/(kg h); M is the maximum dose of drug per kg of body weight per h. Average human body weight is 60 kg, the average body surface area is 1.62 m2, M = 180 mg/m2 × 1.62 m2/60 kg = 4.86 mg/(kg h). Therefore, the endotoxin limit L = 5 EU/(kg h) ÷ 4.86 mg/(kg h) = 1.02 EU/mg. If the irinotecan hydrochloride (nano) micellar infusion time is 30 min, the infusion of calcium folinate with the same time, it should be 30 min, then irinotecan hydrochloride (nano) micelle and calcium folinate should be intravenously administered within 1 h. To ensure the safety of clinical medication for combination therapy, the bacterial endotoxin limit may take half of the above calculated value, that is, less than 0.5 EU/mg.

Monotherapy: The maximum dose of irinotecan hydrochloride (nano) micelles is 350 mg/m2, intravenously administered for more than 90 min, then the maximum dose per kg of body weight per h is M = 350 mg/m2 × 1.62 m2 ÷ 60 kg ÷ 1.5 h = 6.3 mg/(kg h). Therefore, bacterial endotoxin limit for monotherapy treatment is L = 5 EU/ (kg h) ÷ 6.3 mg/(kg h) = 0.794 EU/mg. In order to better ensure the safety of clinical drug use, the bacterial endotoxin limit of this product should be less than 0.5 EU/mg in combination with the results of the bacterial endotoxin limit in the combination therapy. The Maximum Valid Dilution (MVD) is determined by the following calculation: MVD = CL/λ = 10 mg/ml × 0.5 EU/mg ÷ 0.06 EU/ml = 83.

Two bottles of irinotecan hydrochloride (nano) micelles (Batch numbers: 20150325DM, 20150427DM) were resuspended in 4 ml of endotoxin free water to obtain a drug concentration of 10 mg/ml, then to 0.125 mg/ml (diluted 80 times) respectively.

Procedure

The gel-clot LAL procedure follows the Chinese Pharmacopoeia (2015 edition, 1143 instruction for bacterial endotoxin test).

Briefly, the test includes three tests: the confirmation test of the labeled lysate sensitivity, the interfering test, and the endotoxin assessment test.

RPT test

The RPT test was performed according to following procedures in the Chinese Pharmacopoeia 2015 edition (1142 instruction for Rabbit Pyrogen Test).

Briefly, the average temperature of the first two body temperatures was taken as the normal body temperature of rabbits. The sample solution was injected within 15 min after the normal body temperature was measured. Then the body temperature was measured every 30 min, and measured 6 times. The rising temperature of the rabbit body temperature is that the highest body temperature in 6 times minus the normal body temperature.

Result judgment: In three rabbits, the body temperature rise was lower than 0.6 °C, and the total temperature rise of three rabbits was less than 1.3 °C.

Results and discussion

The fabrication and characterization of the nanoformulation have been reported previously [19]. Briefly, the nanoparticles showed a hydrodynamic diameter of 15.1 ± 0.8 nm based on dynamic light scattering and slightly negative surface charge (ζ potential = −4.6 ± 1.3 mV). The encapsulation efficiency of irinotecan hydrochloride of three batches of CPT-11/DSPE-mPEG2000 micelle was assessed to be 90.0% ± 1.0%.

Confirmation test of labeled lysate sensitivity

The results showed in Table A1 demonstrated that 4 batches of Limulus reagent sensitivity determination values are between 0.5λ-2λ, which are eligible for bacterial endotoxin test.

Table A1

Results of Limulus reagent sensitivity confirmation test.

LALSensitivity labeled(EU/ml)	Manufacturer	Lot No.	Endotoxin concentration				Negative control	LALSensitivity measured(EU/ml)
			2λ	λ	0.5λ	0.25λ
0.25	Fuzhou New North Biochemical Industry Co., Ltd.	13121112	++++	++++	– – – –	– – – –	– –	0.25
	Zhanjiang A&C Biological Co., Ltd.	1402261	++++	++++	– – – –	– – – –	– –	0.25
0.06	Zhanjiang A&C Biological Co., Ltd.	1506152	++++	++++	– – – –	– – – –	– –	0.06
	Xiamen Limulus Reagent Experimental Factory Co., Ltd.	150208	++++	++++	– – – –	– – – –	– –	0.06

The ++++ or ---- shows the results for four parallel tests; the ++ or -- shows the results for two parallel tests; + means positive; - means negative.

Interference test

The interference preliminary test (SI) showed that a solution containing 10 mg/ml CPT-11/DSPE-mPEG2000 micelle should be diluted at least 80-fold to a final drug concentration of 0.125 mg/ml to avoid interference with the detection of the endotoxin in the sample.

In the interference test, three groups of samples were tested. First is the endotoxin dissolved in endotoxin free water at different concentrations and the endotoxin free water is the negative control. The second and third groups are 20150325DM and 20150427DM sample solutions at a drug concentration of 0.125 mg/ml spiked with different amounts of endotoxin, respectively. The negative controls for the second and the third groups are 20150325DM and 20150427DM solutions at a drug concentration of 0.125 mg/ml.

The results are listed in Table 1. For both LAL reagents (manufactured by Zhanjiang A&C and Xiamen Limulus Reagent Company), the endotoxin free water showed negative results and the endotoxin positive controls (Group 1) showed the sensitivity of detection ES = λ, indicating that LAL results are valid. However, for samples 20150325DM and 20150427DM, the two kinds of LAL reagents behaved significantly differently. The results from LAL reagent manufactured by Zhanjiang A&C Biological Co., Ltd. showed that with 20150427DM, the sensitivity of detection Et is not between 0.25λ-2λ, which indicated that 0.125 mg/ml sample concentration causes interference for the reaction between LAL reagents and endotoxin. On the other hand, the LAL reagent manufactured by Xiamen Limulus Reagent Experimental Factory Co., Ltd. generated all positive results, including negative controls of samples 20150325DM and 20150427DM. These results demonstrated that at a drug concentration of 0.125 mg/ml, the irinotecan hydrochloride (nano) micelle interferes with the LAL test.

Table 1

Results of irinotecan hydrochloride (nano) micelle interference test.

LALreagentmanufacturer	Solution	Endotoxin concentration				Negative control	The results are calculated
		2λ	λ	0.5λ	0.25λ
Zhanjiang A&C Biological Co., Ltd.	Group 1Endotoxin controla	++++	++++	– – – –	– – – –	– –	ES = λ
	Group 2 20150427DMb	– – – –	– – – –	– – – –	– – – –	– –	Et is not between 0.25λ and 2λ.
	Group 3 20150325DMc	++++	– – – –	– – – –	– – – –	– –	Et = 2λ
Xiamen Limulus Reagent Experimental Factory Co., Ltd.	Group 1Endotoxin controla	++++	++++	– – – –	– – – –	– –	ES = λ
	Group 2 20150427DMb	++++	++++	++++	++++	++	The result is invalid.
	Group 3 20150325DMc	++++	++++	++++	++++	++	The result is invalid.

The ++++ or ---- shows the results for four parallel tests, the ++ or -- shows the results for two parallel tests, + means positive, -means negative.

Endotoxin control: endotoxin and endotoxin test with aqueous solution, the negative control for endotoxin water.

20150427DM: 0.125 mg/ml of the addition of endotoxin 20150427DM solution, the negative control was endotoxin test water.

20150325DM: 0.125 mg/ml of 20150325DM solution added with endotoxin, and the negative control is 0.125 mg/ml of 20150325DM solution.

The sensitivity of LAL used in the current test is 0.06 EU/ml. If we further dilute the sample to 0.0625 mg/ml, the only choice would be the LAL reagent with a sensitivity of 0.03 EU/ml, which is the most sensitive LAL reagent available in China. Considering the risk of different test results due to the different batches of LAL reagents from different manufacturers or different batches of samples at a concentration of 0.0625 mg/ml, we concluded that LAL method is not suitable for bacterial endotoxin detection of this product. It has been reported in literature that some materials such as detergents or proteins may enhance or inhibit the interaction of LPS with the LAL reagent, causing false positive or negative results [13]. The amphiphilic DSPE-mPEG2000 can also be regarded as a detergent and may interfere with the test results.

To test the interference of empty micelle to body temperature increase of rabbits, we performed a preliminary experiment. Empty micelle (batch 20150323EM) was diluted with 5% glucose injection solution to prepare a micelle solution of 12.0 mg/ml, which corresponds to a drug concentration of 2.8 mg/ml (maximum injection concentration) in drug-containing micelles. Each rabbit was injected with 10 ml of the solution per kg of body weight. All the procedures in this test followed the Chinese Pharmacopoeia (2015 edition, fourth part, 1142 pyrogen test method). The results are listed in Table 2. In three rabbits, the body temperature rise was lower than 0.6 °C, and the total temperature rise of three rabbits was less than 1.3  °C. It showed that the empty micelles did not increase the body temperature of rabbits, and proved that the excipients used in the formulation did not interfere with the pyrogen test.

Table 2

Results of empty micellar pyrogen test.

Drug name: empty micelle						Drug lot number: 20150323EM
Rabbit No.	BT1(°C)	BT2(°C)	Initial BTAvg(°C)	BT3(°C)	BT4(°C)	BT5(°C)	BT6(°C)	BT7(°C)	BT8(°C)	ΔBT(+)(°C)	ΔBT(−)(°C)
1	38.90	39.06	38.98	39.34	39.18	39.18	39.06	39.10	39.06	0.36	0.00
2	38.92	38.96	38.94	39.11	38.92	39.04	39.19	39.15	39.19	0.25	−0.02
3	38.54	38.57	38.56	38.42	38.54	38.61	38.69	38.65	38.61	0.13	−0.14

Total temperature rise: 0.74 °C.

We then conducted the test with three batches of irinotecan hydrochloride (nano) micelles 20150325DM, 20150427DM, and 20150624DM and the commercially available irinotecan hydrochloride injection as a control (trade name Campto, batch HR83C). The above samples were dissolved in a 5% glucose solution at a drug concentration of 2.8 mg/ml and 10 ml/kg body weight, and then injected into the rabbits. The results in Table 3, Table 4, Table 5, Table 6 showed that both the commercial irinotecan hydrochloride injection and irinotecan hydrochloride (nano) micelles did not cause the rabbit body temperature to rise. On the contrary, we observed that three batches of irinotecan hydrochloride (nano) micelles decreased the body temperature of rabbits by 2.85, 2.69 and 2.16 °C, respectively (the sum of temperature decrease). A similar trend was observed with the commercial irinotecan hydrochloride injection during the test period in the rabbits (4.12 °C). These results taken together suggested that irinotecan hydrochloride the drug itself at a dosage of 28 mg/kg can lead to a decrease in body temperature in rabbits. This not only causes discomfort in the animals involved in the test, but also may neutralize the warming effect of pyrogen, rendering the conclusions ambiguous in determination of the endotoxin content and safety of the products. The irinotecan hydrochloride has already been reported to induce acute hypothermia effect in mice which gradually recover subsequently and this effect on body temperature is irrelevant of sex of the animals [20]. In addition, other drugs including amifostine and breviscapin have also been reported to exhibit similar effect of reducing animal body temperature during pyrogen test and potentially interfering with the accuracy of the results [21], [22]. In the two cases mentioned above, LAL test was used instead of the pyrogen test to avoid these issues.

Table 3

Pyrogen test results of irinotecan hydrochloride (nano) micelles (high dose).

Drug name: irinotecan hydrochloride injection						Lot number: HR83C
Rabbit No.	BT1(°C)	BT2(°C)	Initial BTAvg(°C)	BT3(°C)	BT4(°C)	BT5(°C)	BT6(°C)	BT7(°C)	BT8(°C)	ΔBT(+)(°C)	ΔBT(−)(°C)
4	38.36	38.40	38.38	37.03	37.27	37.71	37.95	38.07	38.40	0.02	−1.35
5	39.27	39.42	39.35	38.05	38.31	38.56	38.75	38.93	39.08	0.00	−1.30
6	38.93	38.97	38.95	37.48	37.81	37.93	38.12	38.12	38.27	0.00	−1.47

Total temperature rise: 0.02 °C.

Table 4

Pyrogen test results of irinotecan hydrochloride (nano) micelles (high dose).

Drug name: irinotecan hydrochloride for injection (nano) micelles						Lot number: 20150325DM
Rabbit No.	BT1(°C)	BT2(°C)	Initial BTAvg(°C)	BT3(°C)	BT4(°C)	BT5(°C)	BT6(°C)	BT7(°C)	BT8(°C)	ΔBT(+)(°C)	ΔBT(−)(°C)
7	38.48	38.40	38.44	37.69	38.07	38.22	38.40	38.52	38.71	0.27	−0.75
8	38.84	38.80	38.82	38.19	38.61	38.77	38.84	38.73	38.69	0.02	−0.63
9	39.04	38.96	39.00	37.53	37.79	38.09	38.20	38.39	38.65	0.00	−1.47

Total temperature rise: 0.29 °C.

Table 5

Pyrogen test results of irinotecan hydrochloride (nano) micelles (high dose).

Drug name: irinotecan hydrochloride for injection (nano) micelles						Lot number: 20150427DM
Rabbit No.	BT1(°C)	BT2(°C)	Initial BTAvg(°C)	BT3(°C)	BT4(°C)	BT5(°C)	BT6(°C)	BT7(°C)	BT8(°C)	ΔBT(+)(°C)	ΔBT(−)(°C)
10	38.86	38.79	38.83	38.45	38.20	37.84	37.37	37.37	37.73	0.00	−1.46
11	38.46	38.54	38.50	38.81	38.70	38.42	38.50	38.50	38.66	0.31	−0.08
12	38.90	38.71	38.81	38.29	37.99	37.66	37.80	37.80	38.29	0.00	−1.15

Total temperature rise: 0.31 °C.

Table 6

Pyrogen test results of irinotecan hydrochloride (nano) micelles (high dose).

Drug name: irinotecan hydrochloride for injection (nano) micelles						Lot number: 20150624DM
Rabbit No.	BT1(°C)	BT2(°C)	Initial BTAvg(°C)	BT3(°C)	BT4(°C)	BT5(°C)	BT6(°C)	BT7(°C)	BT8(°C)	ΔBT(+)(°C)	ΔBT(−)(°C)
13	38.85	38.85	38.85	37.99	37.75	37.87	37.87	38.03	38.20	0.00	−1.10
14	38.53	38.49	38.51	38.45	38.27	38.20	38.13	38.27	38.42	0.00	−0.38
15	39.05	39.05	39.05	39.13	38.94	38.48	38.37	38.48	38.63	0.08	−0.68

Total temperature rise: 0.08 °C.

To overcome the body temperature decreasing effect of irinotecan hydrochloride, we reduced the injection dose. The samples were then prepared at a drug concentration of 11 mg/ml and the rabbits were injected with 1 ml per kg of body weight. The results are shown in Table 7, Table 8, Table 9. At this injection dosage, three batches of irinotecan hydrochloride (nano) micelles including 20150325DM, 20150427DM and 20150624DM did not raise the temperature of the rabbits more than the chinese pharmacopoeia required and the result of the pyrogen test can be regarded as passed.

Table 7

Pyrogen test results of irinotecan hydrochloride (nano) micelles (low dose).

Drug name: irinotecan hydrochloride for injection (nano) micelles						Lot number: 20150325DM
Rabbit No.	BT1(°C)	BT2(°C)	Initial BTAvg(°C)	BT3(°C)	BT4(°C)	BT5(°C)	BT6(°C)	BT7(°C)	BT8(°C)	ΔBT(+)(°C)	ΔBT(−)(°C)
16	39.07	39.03	39.05	38.84	38.81	38.77	38.73	38.84	38.96	0.00	−0.32
17	38.71	38.79	38.75	38.75	38.79	38.87	38.79	39.06	38.98	0.31	−0.00
18	39.00	39.00	39.00	39.08	39.00	38.93	38.89	38.89	38.97	0.08	−0.11

Total temperature rise: 0.39 °C.

Table 8

Pyrogen test results of irinotecan hydrochloride (nano) micelles (low dose).

Drug name: irinotecan hydrochloride for injection (nano) micelles						Lot number: 20150427DM
Rabbit No.	BT1(°C)	BT2(°C)	Initial BTAvg(°C)	BT3(°C)	BT4(°C)	BT5(°C)	BT6(°C)	BT7(°C)	BT8(°C)	ΔBT(+)(°C)	ΔBT(−)(°C)
19	38.86	38.90	38.88	37.78	38.66	38.74	38.78	38.78	38.86	0.00	−0.22
20	38.71	38.75	38.73	38.79	38.68	38.56	38.71	38.75	38.94	0.21	−0.17
21	38.99	38.99	38.99	38.87	38.83	38.76	38.68	38.76	38.83	0.00	−0.31

Total temperature rise: 0.21 °C.

Table 9

Pyrogen test results of irinotecan hydrochloride (nano) micelles (low dose).

Drug name: irinotecan hydrochloride for injection (nano) micelles						Lot number: 20150624DM
Rabbit no.	BT1°C	BT2°C	Initial BTAvg°C	BT3°C	BT4°C	BT5°C	BT6°C	BT7°C	BT8°C	ΔBT(+)°C	ΔBT(−)°C
22	38.87	38.84	38.86	38.87	38.72	38.76	38.80	38.87	38.91	0.05	−0.14
23	38.75	38.71	38.73	38.59	38.47	38.43	38.43	38.47	38.51	0.00	−0.30
24	38.71	38.75	38.73	37.94	38.97	39.12	39.05	39.08	39.12	0.39	−0.00

Total temperature rise: 0.44 °C.

It is mentioned in literature that 3-10 times the injection dosage used in the clinics based on weight is recommended for pyrogen test, as long as the drug does not interfere with the physical wellness of the rabbit [23]. Based on this, the dosage should be 33.6-112 mg/kg. In the first test, we used the highest concentration of the drug used in the clinics (2.8 mg/ml) and injected the rabbit with the largest volume of drug solution (10 ml), to ensure the safety of the nanoformulation. Since there is no clear direction on the dosage given to the animals in pyrogen test in the chinese pharmacopoeia, reducing the dosage to 11 mg/kg which is equal to the injection dosage used in the clinics based on weight, to avoid the hypothermia effect of the irinotecan hydrochloride might be acceptable. However, these issues call into question the relevance of RPT and drug safety in humans and may result in complex situation where the drug passes RPT, but causes fever in patients.

Meanwhile, drug-loaded nanoparticles are more complex than pure drugs, so it is necessary to detect the endotoxin of the preparations before clinical practice. This work will provide reference for experimental and clinical research of nanomedicines.

Conclusion

Pyrogenicity/endotoxin detection is an important step in characterization of nanomaterials for preclinical study. With more and more nanoformulation entering clinical study, the necessity to accurately detect the pyrogen is increasing. Here we presented the endotoxin detection results from the characterization of a CPT-11/DSPE-mPEG2000 (nano) micelle formulation which has been declared clinically.

Firstly, formulation of drugs into nanosized particles introduces components that have never been used in pharmaceutics and may render the current LAL method not applicable. In this study, we found that the CPT-11/DSPE-mPEG2000 (nano) micelle causes interference with the detection of the endotoxin using gel-clot format LAL assay. Secondly, the irinotecan hydrochloride drug itself at a dose of 28 mg/kg causes a hypothermia effect in the rabbits which forces us to reduce the dose to 11 mg/kg. So it is necessary to develop new methods to overcome these issues that may interfere with accurate evaluation of endotoxin content. New biosensors such as electrochemical biosensors, optical biosensors and mass-based biosensors may be considered as promising strategies for endotoxin detection. Because of their miniaturization, low cost, and high sensitivity, their release into market will be obvious success.

Conflicts of interest

The authors declare that there are no conflicts of interest. The authors alone are responsible for the content and writing of this article.

Table A2

Results of irinotecan hydrochloride (nano) micellar interference pretest.

Sample dilution	Fuzhou New North Biochemical Industry Co., Ltd.		Zhanjiang A&C Biological Co., Ltd.
	Sample	Positive control	Sample	Positive control
10×	– –	– –	– –	– –
20×	– –	– –	– –	– –
40×	– –	++	– –	– –
80×	– –	++	– –	++
160×	– –	++	– –	++

The ++ or -- shows the results for two parallel tests; + means positive; - means negative.